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Database: 365,228(8 Aug 2026)

liquid serum

liquid serum, Total:471 items.

The international standard classification for "liquid serum" includes: Protection against crime , Surgical instruments and materials , Laboratory medicine , Implants for surgery, prosthetics and orthotics , Other medical equipment , Medical Sciences and health care facilities in general , Transfusion, infusion and injection equipment .

The Chinese standard classification for "liquid serum" includes: Crime judging technology , Extracorporeal circulation, artificial organ and prosthesis device , Medical laboratory equipment , Sanitation in general , General and microsurgical devices , Legal medical expert .


Guangdong Provincial Standard of the People's Republic of China

Professional Standard - Public Safety Standards

  • GA/T 1633-2019 Forensic sciences—Examination methods for ethyl glucuronide in blood and urine samples—GC-MS and LC-MS
  • GA/T 1632-2019 Forensic sciences—Examination methods for mepiquat and chlormequat in blood and urine samples—LC-MS
  • GA 475-2004 Serum product of anti-human serum
  • GA/T 1320-2016 GC-MS examination methods for fluoride ion in urine and blood in forensic science
  • GA 472-2004 Serum product of anti-human hemoglobin
  • GA/T 1629-2019 Paraquat detection in blood and urine for forensic science by gas chromatography and gas chromatography-mass spectrometry
  • GA 473-2004 Serum products of anti-human semen

Professional Standard - Medicine

  • YY 0793.2-2023 Preparation and quality management of fluids for haemodialysis and related therapies--Part 2:Water for haemodialysis and related therapies
  • YY/T 0598-2015 Concentrates for haemodialysis and related therapies
  • YY 0053-2016 Hemodialysis and relavant therapics -Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • YY 0793.3-2023 Preparation and quality control of fluids for hemodialysis and related treatments - Part 3: Concentrates for hemodialysis and related treatments
  • YY 0598-2015(A1) Concentrates for haemodialysis and related therapies
  • YY/T 1920-2023 Blood compatibility tests of haemodialysers
  • YY 0598-2006 Concentrates for haemodialysis and related therapies
  • YY/T 0456.1-2014 Reagents for hematology analyzer―Part 1:Rinse
  • YY 0053-2008 Cardiovascular implants and artificial organs—Haemodialysers haemodiafilters haemofilters and haemoconcentrators
  • YY 0572-2015 Water for haemodialysis and related therapies
  • YY/T 0456.1-2003 Regents for hematology analyzer use - Part 1: Rinse
  • YY 0054-2003 Haemodialysis、haemodiafiltration and haemofiltration equipment
  • YY 0598-2015 Concentrates for haemodialysis and related therapies
  • YY 0572-2005 Water for haemodialysis and related therapies
  • YY 0267-2016 Hemodialysis and related therapies―Extracorporeal blood circuit for blood purification devices

未注明发布机构

  • CSA Z23500-2-2020 Preparation and quality management of fluids for haemodialysis and related therapies — Part 2: Water treatment equipment for haemodialysis applications and related therapies
  • DIN EN 1283:1996 Hemodialyzers, hemodiafilters, hemofilters, hemoconcentrators and associated LJ blood tubing systems
  • DIN EN ISO 8637 E:2013-06 Cardiovascular implants and extracorporeal systems Hemodialyzers, hemodialysis filters, hemofilters and hemoconcentrators (draft)
  • DIN EN ISO 13959 E:2015-04 Water for hemodialysis and related treatments (draft)
  • DIN EN ISO 8637-2 E:2023-01 Extracorporeal systems for blood purification Part 2: Extracorporeal blood circuits for hemodialyzers, hemodiafilters and hemofilters (draft)
  • ANSI/AAMI/ISO 8637-2:2018 Extracorporeal systems for blood purification— Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • ANSI/AAMI/ISO 8637-1:2017 Extracorporeal systems for blood purification— Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • CAN/CSA-Z8637-2008 Cardiovascular Implants and Artificial Organs - Haemodialysers, Haemodiafilters, Haemofilters and Haemoconcentrators
  • DIN EN ISO 8638 E:2013-06 Cardiovascular implants and extracorporeal systems Hemodialyzers, hemodiafilters and hemofilters for extracorporeal circulation (draft)
  • ANSI/AAMI/ISO 23500-2:2019 Preparation and quality management of fluids for haemodialysis and related therapies—Part 2: Water treatment equipment for haemodialysis applications and related therapies
  • ANSI/AAMI/ISO 23500-4:2019 Preparation and quality management of fluids for haemodialysis and related therapies— Part 4: Concentrates for haemodialysis and related therapies
  • CSA ISO 8637-2:2021 Extracorporeal systems for blood purification — Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • CSA Z23500-3-2020 Preparation and quality management of fluids for haemodialysis and related therapies — Part 3: Water for haemodialysis and related therapies
  • CAN/CSA-Z8638-2008 Cardiovascular Implants and Artificial Organs - Extracorporeal Blood Circuit for Haemodialysers, Haemodiafilters and Haemofilters
  • ANSI/AAMI/ISO 23500-5:2019 Preparation and quality management of fluids for haemodialysis and related therapies—Part 5: Quality of dialysis fluid for haemodialysis and related therapies
  • ANSI/AAMI/ISO 23500-3:2019 Preparation and quality management of fluids for haemodialysis and related therapies—Part 3: Water for haemodialysis and related therapies
  • DIN 58931 E:2021-02 Haematology - Determination of haemoglobin concentration in blood - Reference method
  • DIN EN ISO 8637-2 E:2016-05 Extracorporeal systems for blood purification Part 2: Extracorporeal blood circuits for hemodialyzers, hemodiafilters and hemofilters (draft)
  • ANSI/AAMI/ISO 8638:2010(2015) Cardiovascular implants and extracorporeal systems — Extracorporeal blood circuit for hemodialyzers, hemodiafilters and hemofilters
  • DIN EN ISO 13958 E:2015-05 Concentrates for hemodialysis and related therapies (draft)
  • DIN EN ISO 8637-1 E:2016-05 Extracorporeal systems for blood purification Part 1: Hemodialyzers, hemodialysis filters, hemofilters and hemoconcentrators (draft)
  • DIN 58931 E:2009-03 Haematology - Determination of haemoglobin concentration in blood - Reference method
  • CSA Z23500-5-2020 Preparation and quality management of fluids for haemodialysis and related therapies — Part 5: Quality of dialysis fluid for haemodialysis and related therapies
  • DIN EN ISO 11663 E:2015-05 Quality of dialysate for hemodialysis and related treatments (draft)

Group Standards of the People's Republic of China

  • T/SHSYCXH 11-2022 Determination of free amino acids in serum—Liquid chromatography tandem mass spectrometry
  • T/GDC 169-2022 Disposable plastic serological pipet
  • T/BDAS 002-2023 Determination of melatonin content in serum— Liquid chromatography-tandem mass spectrometry
  • T/ZZB 1652-2020 Disposable serological pipettes(Polystyrene)
  • T/CADERM 3026-2020 Specifications for diagnosis and treatment of serum sickness

Professional Standard - Hygiene

  • WS/T 478-2015 Operating guidelines for measurement of serum 25-hydroxvitamin D3-Isotope dilution liquid chromatography tandem mass spectrometry
  • WS/T 412-2013 Reference measurement method for serum triglycerides-Isotope dilution gas chromatography mass spectrometry
  • WS/T 413-2013 Reference mesurement method for serum creatinine-Isotope dilution liquid chromatography tandem mass spectrometry
  • WS/T 478-2024 Determination of serum 25-hydroxyvitamin D2 and D3 by isotope dilution liquid chromatography tandem mass spectrometry
  • WS/T 355-2011 Guidelines for enzymatic measurements of serum triglycerides
  • WS/T 413-2024 Reference procedure for measurement of serum creatinine by isotope dilution liquid chromatography tandem mass spectrometry
  • WS/T 463-2015 Measurement of serum low density lipoprotein cholesterol

国家药监局

  • YY/T 1631.2-2020 Compatibility determination of the transfusion sets with blood component—Part 2:Assessment of damage to blood component
  • YY/T 1631.1-2018 Compatibility determination of the transfusion sets with blood components―Part 1:Assessment of blood component depletion
  • YY/T 0793.1-2022 Preparation and quality management for liquid used in haemodialysis and related therapies—Part 1: Water treatment equipments for haemodialysis and related therapies
  • YY/T 0793.4-2022 Preparation and quality management of fluids for hacmodialysis andrelated therapics—Part 1:Water treatment equipment for haemodialysis applications and related therapies

National Health Commission of the People's Republic of China

  • WST 355:2011 Enzymatic determination of serum triglycerides (obsolete)

Anhui Provincial Standard of the People's Republic of China

  • DB34/T 3861-2021 Determination of AFB1 biomarker in serum high performance liquid chromatographic method

Taiwan Provincial Standard of the People's Republic of China

  • CNS 14193-1998 Haemodialysers,hasmofilters and haemoconcentrators
  • CNS 14194-1998 Extracorporeal blood circuit for haemodialysers hasmofilters and haemoconcentrators

General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China

  • GB/T 13074-1991 Terms of blood purification Hemodialysis and hemofiltration

Professional Standard - Agriculture

国家食品药品监督管理局

  • YY/T 1422-2016 Pregnancy-associated plasma protein A (PAPP-A) in serum test reagent (quantitative labelling immunoassay)

Jilin Provincial Standard of the People's Republic of China

  • DB22/T 3049-2019 Determination of Six Mushroom Toxins in Blood and Urine by Liquid Chromatography-Tandem Mass Spectrometry

Agricultural Standard of the People's Republic of China

司法部

  • SF/T 0113-2021 Determination of cyanide in blood by gas chromatography-mass spectrometry and gas chromatography

IN-BIS

  • IS 4364-1967 Pipette Specifications Serology
  • IS 13878-1993 Extracorporeal blood circuit for haemodialysers, haemofilters and haemoconcentrators - specification
  • IS 13890-1994 Haemodialysers, haemofilters and haemoconcentrators - specification

SCC

  • BS 7297-1:1990 Haemodialysers and related equipment-Specification for haemodialysers, haemofilters and haemoconcentrators
  • BS 7297-2:1990 Haemodialysers and related equipment-Specification for extracorporeal circuits for use with haemodialysers, haemofilters and haemoconcentrators
  • AAMI/ISO 13959:2009 Water for hemodialysis and related therapies
  • AENOR UNE 23056:1971 BLOOD TRANSFUSION. WITNESS SERUMS
  • AENOR UNE-EN 13867+A1:2009 Concentrates for hemodialysis and related therapies.
  • AAMI 13959:2014 Water for hemodialysis and related therapies
  • DANSK DS/EN ISO 13959:2015 Water for haemodialysis and related therapies
  • CAN/CSA Z364.1.1/Z364.1.2-1994(R2006) Haemodialysers, Haemofilters and Haemoconcentrators/ Extracorporeal Blood Circuit for Haemodialysers, Haemofilters and Haemoconcentrators
  • AAMI/ISO 23500-4:2019 Preparation and quality management of fluids for haemodialysis and related therapies – Part 4: Concentrates for haemodialysis and related therapies
  • CAN/CSA-ISO 13959-11:2011 Water for haemodialysis and related therapies
  • CAN/CSA-Z902-2010 Blood and blood components
  • DANSK DS/ISO 23500-4:2019 Preparation and quality management of fluids for haemodialysis and related therapies – Part 4: Concentrates for haemodialysis and related therapies
  • CAN/CSA Z902-2004 Blood and Blood Components
  • CAN/CSA-Z902-2004(R2009) Blood and Blood Components
  • DANSK DS/ISO 23500-3:2019 Preparation and quality management of fluids for haemodialysis and related therapies – Part 3: Water for haemodialysis and related therapies
  • AAMI 11663:2014 Quality of dialysis fluid for hemodialysis and related therapies
  • CAN/CSA-ISO 11663-11:2011 Quality of dialysis fluid for haemodialysis and related therapies
  • DANSK DS/ISO 23500-5:2019 Preparation and quality management of fluids for haemodialysis and related therapies – Part 5: Quality of dialysis fluid for haemodialysis and related therapies
  • NS-EN ISO 23500-4:2019 Preparation and quality management of fluids for haemodialysis and related therapies - Part 4: Concentrates for haemodialysis and related therapies (ISO 23500-4:2019)
  • AAMI/ISO 11663:2009 Quality of dialysis fluid for hemodialysis and related therapies
  • 08/30179595 DC BS ISO 13958. Concentrates for haemodialysis and related therapies
  • DANSK DS/EN ISO 11663:2015 Quality of dialysis fluid for haemodialysis and related therapies
  • AAMI/ISO 23500-3:2019 Preparation and quality management of fluids for haemodialysis and related therapies – Part 3: Water for haemodialysis and related therapies
  • AAMI/ISO 23500-5:2019 Preparation and quality management of fluids for haemodialysis and related therapies – Part 5: Quality of dialysis fluid for haemodialysis and related therapies
  • 13/30270468 DC BS ISO 13958. Concentrates for haemodialysis and related therapies
  • CAN/CSA-Z364.1.1-1994(C2006) Hemodialyzers, hemofilters and hemoconcentrators
  • CAN/CGSB-106.1-M86-1986 Serums for blood group determination
  • DANSK DS/EN ISO 23500-4:2019 Preparation and quality management of fluids for haemodialysis and related therapies – Part 4: Concentrates for haemodialysis and related therapies (ISO 23500-4:2019)
  • NS-EN ISO 23500-4:2024 Preparation and quality management of fluids for haemodialysis and related therapies - Part 4: Concentrates for haemodialysis and related therapies (ISO 23500-4:2024)
  • CAN 3-Z364.1.1-M84-1984 Hemodialyzers, hemofilters and hemoconcentrators
  • CAN/CSA-Z364.1.1-1994(R2006) Haemodialysers, Haemofilters and Haemoconcentrators
  • AAMI TIR43:2021 Ultrapure dialysis fluid for hemodialysis and related therapies
  • CAN/CSA-Z364.1.2-1994(C2006) Extracorporeal blood circuit for hemodialyzers, hemofilters and hemoconcentrators
  • DANSK DS/EN ISO 8637-1:2021 Extracorporeal systems for blood purification – Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • AAMI TIR43:2011 Ultrapure dialysate for hemodialysis and related therapies
  • CAN/CSA-Z364.1.2-1994(R2006) Extracorporeal Blood Circuit for Haemodialysers, Haemofilters and Haemoconcentrators
  • 13/30270465 DC BS ISO 11663. Quality of dialysis fluid for haemodialysis and related therapies
  • NS-EN 1283:1996 Haemodialysers, haemodiafilters, haemofilters, haemoconcentrators and their extracorporeal circuits
  • NS-EN ISO 23500-5:2019 Preparation and quality management of fluids for haemodialysis and related therapies - Part 5: Quality of dialysis fluid for haemodialysis and related therapies (ISO 23500-5:2019)
  • 13/30270471 DC BS ISO 13959. Water for haemodialysis and related therapies
  • 08/30179572 DC BS ISO 11663. Quality of dialysis fluid for haemodialysis and related therapies
  • UNE-EN 1283:1996 HAEMODIALYSERS, HAEMODIAFILTERS, HAEMOFILTERS, HAEMOCONCENTRATORS AND THEIR EXTRACORPOREAL CIRCUITS.
  • DANSK DS/ISO 23500-2:2019 Preparation and quality management of fluids for haemodialysis and related therapies – Part 2: Water treatment equipment for haemodialysis applications and related therapies
  • DANSK DS/EN ISO 23500-3:2019 Preparation and quality management of fluids for haemodialysis and related therapies – Part 3: Water for haemodialysis and related therapies (ISO 23500-3:2019)
  • 08/30179598 DC BS ISO 13959. Water for haemodialysis and related therapies
  • NS-EN ISO 23500-5:2024 Preparation and quality management of fluids for haemodialysis and related therapies - Part 5: Quality of dialysis fluid for haemodialysis and related therapies (ISO 23500-5:2024)
  • NS-EN ISO 13959:2015 Water for haemodialysis and related therapies (ISO 13959:2014)
  • CSA Z902-15:2015 Blood and labile blood products
  • AAMI/ISO 23500-2:2019 Preparation and quality management of fluids for haemodialysis and related therapies – Part 2: Water treatment equipment for haemodialysis applications and related therapies
  • AAMI RD16:2007 Cardiovascular implants and artificial organs - Hemodialyzers, hemodiafilters, hemofilters and hemoconcentrators
  • NS-EN ISO 23500-3:2019 Preparation and quality management of fluids for haemodialysis and related therapies — Part 3: Water for haemodialysis and related therapies (ISO 23500-3:2019)
  • DANSK DS/EN ISO 23500-5:2019 Preparation and quality management of fluids for haemodialysis and related therapies – Part 5: Quality of dialysis fluid for haemodialysis and related therapies (ISO 23500-5:2019)
  • AAMI/ISO 8637-1:2017 Extracorporeal systems for blood purification - Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • AAMI/ISO 13958:2009 Concentrates for hemodialysis and related therapies
  • AENOR UNE 23051:1971 BLOOD TRANSFUSION. LIQUID HUMAN BLOOD PLASMA
  • AAMI/ISO 8637-2:2018 Extracorporeal systems for blood purification - Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • NS-EN 13867:2002+A1:2009 Concentrates for haemodialysis and related therapies
  • DANSK DS/EN ISO 8637:2014 Cardiovascular implants and extracorporeal systems – Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • AAMI 13958:2014 Concentrates for hemodialysis and related therapies
  • CAN/CSA-ISO 8637-2-2021 Extracorporeal systems for blood purification – Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (ISO 8637-2:2018, IDT)
  • NS-EN ISO 8637-1:2020 Extracorporeal systems for blood purification — Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637-1:2017)
  • DANSK DS/EN ISO 13958:2015 Concentrates for haemodialysis and related therapies
  • NS-EN 13867:2002 Concentrates for haemodialysis and related therapies
  • NS-EN ISO 11663:2015 Quality of dialysis fluid for haemodialysis and related therapies (ISO 11663:2014)
  • UNE-EN 13867:2003 Concentrates for haemodialysis and related therapies.
  • UNE-EN 13867:2003+A1:2009 Concentrates for haemodialysis and related therapies
  • CAN/CSA-ISO 13958-11:2011 Concentrates for haemodialysis and related therapies
  • DANSK DS/EN ISO 8637-2:2018 Extracorporeal systems for blood purification – Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (ISO 8637-2:2018)
  • DIN EN ISO 23500-3 E:2017 Draft Document - Guidance for the preparation and quality management of fluids for haemodialysis and related therapies - Part 3: Water for haemodialysis and related therapies (ISO/DIS 23500-3:2017); German and English version prEN ISO 23500-3:2017
  • DIN EN ISO 23500-4 E:2017 Draft Document - Guidance for the preparation and quality management of fluids for haemodialysis and related therapies - Part 4: Concentrates for haemodialysis and related therapies (ISO/DIS 23500-4:2017); German and English version prEN ISO 23500-4:2017
  • AENOR UNE-EN 13867:2003 Concentrates for hemodialysis and related therapies.
  • BS PD CEN/TS 16945:2016 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for metabolomics in urine, venous blood serum and plasma
  • NS-EN ISO 8637-2:2018 Extracorporeal systems for blood purification - Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (ISO 8637-2:2018)
  • CAN/CSA-ISO 8637-1-2021 Extracorporeal systems for blood purification – Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637-1:2017, IDT)
  • NS-EN ISO 23500-2:2019 Preparation and quality management of fluids for haemodialysis and related therapies - Part 2: Water treatment equipment for haemodialysis applications and related therapies (ISO 23500-2:2019)
  • AENOR UNE-EN ISO 11663:2016 Quality of dialysis fluid for haemodialysis and related therapies (ISO 11663:2014)
  • AENOR UNE-EN ISO 13959:2016 Water for hemodialysis and related therapies. (ISO 13959:2014).
  • CAN 3-Z364.1.2-M84-1984 Extracorporeal circuits for hemodialyzers, hemofilters and hemoconcentrators
  • AAMI/ISO RD17:2007 Cardiovascular implants and artificial organs - Extracorporeal blood circuit for hemodialyzers, hemodiafilters and hemofilters
  • AS 3864:1991 Medical refrigeration equipment - For the storage of blood and blood products, and containers for the transport of blood and blood products
  • DANSK DS/EN ISO 8638:2014 Cardiovascular implants and extracorporeal systems – Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • DIN EN ISO 8637-1 E:2016 Draft Document - Extracorporeal systems for blood purification - Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO/DIS 8637-1:2016); German and English version prEN ISO 8637-1:2016
  • DIN EN ISO 23500-5 E:2017 Draft Document - Guidance for the preparation and quality management of fluids for haemodialysis and related therapies - Part 5: Quality of dialysis fluid for haemodialysis and related therapies (ISO/DIS 23500-5:2017); German and English version prEN I...
  • DIN EN ISO 8637 E:2013 Draft Document - Cardiovascular implants and extracorporeal systems - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637:2010); German version FprEN ISO 8637:2013
  • DIN EN ISO 8637-2 E:2016 Draft Document - Extracorporeal systems for blood purification - Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (ISO/DIS 8637-2:2016); German and English version prEN ISO 8637-2:2016
  • DIN EN ISO 13959 E:2015 Draft Document - Water for haemodialysis and related therapies (ISO 13959:2014); German and English version FprEN ISO 13959:2015
  • DANSK DS/ISO 23118:2021 Molecular in vitro diagnostic examinations – Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
  • AENOR UNE-EN ISO 8638:2014 Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (ISO 8638:2010)
  • CEI EN 60601-2-16:2018 Electrical medical equipment Part 2: Particular requirements relating to the basic safety and essential performance of hemodialysis, hemodiafiltration and haemofiltration equipment
  • BS EN ISO 23500:2015 Guidance for the preparation and quality management of fluids for haemodialysis and related therapies
  • NS-EN ISO 8638:2014 Cardiovascular implants and extracorporeal systems — Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (ISO 8638:2010)
  • DANSK DS/CEN/TS 16945:2016 Molecular in vitro diagnostic examinations – Specifications for pre-examination processes for metabolomics in urine, venous blood serum and plasma
  • SN-CEN/TS 16945:2016 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for metabolomics in urine, venous blood serum and plasma
  • ISO/DIS 13959:1997 Water for Haemodialysis or Haemodiafiltration - Requirements
  • AENOR UNE 23049:1971 BLOOD TRANSFUSION. PRESERVED HUMAN BLOOD
  • CAN/CSA-Z23500-2012 Guidelines for the preparation and quality management of fluids for hemodialysis and related therapies
  • DANSK DS/EN ISO 23500:2015 Guidance for the preparation and quality management of fluids for haemodialysis and related therapies
  • BS ISO 23500:2011 Guidance for the preparation and quality management of fluids for haemodialysis and related therapies
  • DIN EN ISO 8638 E:2013 Draft Document - Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (ISO 8638:2010); German version FprEN ISO 8638:2013
  • AAMI/ISO 23500:2011 Guidance for the preparation and quality management of fluids for hemodialysis and related therapies
  • AAMI 23500:2014 Guidance for the preparation and quality management of fluids for hemodialysis and related therapies
  • DIN 58905-1 E:2015 Draft Document - Haemostaseology - Blood collection - Part 1: Preparation of plasma from citrated venous blood for coagulation testing; Text in German and English
  • DANSK DS/EN ISO 23500-2:2019 Preparation and quality management of fluids for haemodialysis and related therapies – Part 2: Water treatment equipment for haemodialysis applications and related therapies (ISO 23500-2:2019)

British Standards Institution (BSI)

  • BS EN ISO 23500-4:2024 Preparation and quality management of fluids for haemodialysis and related therapies - Concentrates for haemodialysis and related therapies
  • BS 6706:1986(2011) Specification for Disposable glass serological pipettes
  • BS EN ISO 23500-3:2024 Preparation and quality management of fluids for haemodialysis and related therapies - Water for haemodialysis and related therapies
  • BS EN ISO 23500-3:2019 Preparation and quality management of fluids for haemodialysis and related therapies. Water for haemodialysis and related therapies
  • BS ISO 13959:2014 Water for haemodialysis and related therapies
  • BS ISO 13959:2009 Water for haemodialysis and related therapies
  • BS EN ISO 13959:2015 Water for haemodialysis and related therapies
  • BS EN ISO 23500-5:2019 Preparation and quality management of fluids for haemodialysis and related therapies. Quality of dialysis fluid for haemodialysis and related therapies
  • BS EN ISO 23500-5:2024 Preparation and quality management of fluids for haemodialysis and related therapies - Quality of dialysis fluid for haemodialysis and related therapies
  • BS ISO 12771:1997(1999) Plastics Laboratory Ware — Disposable serological pipettes
  • BS EN ISO 11663:2015 Quality of dialysis fluid for haemodialysis and related therapies
  • BS EN ISO 23500-4:2019 Preparation and quality management of fluids for haemodialysis and related therapies. Concentrates for haemodialysis and related therapies
  • BS EN ISO 23500-2:2024 Preparation and quality management of fluids for haemodialysis and related therapies - Water treatment equipment for haemodialysis applications and related therapies
  • BS ISO 11663:2014 Quality of dialysis fluid for haemodialysis and related therapies
  • BS ISO 11663:2009 Quality of dialysis fluid for haemodialysis and related therapies
  • 22/30449717 DC BS EN ISO 23500-4. Preparation and quality management of fluids for haemodialysis and related therapies - Part 4. Concentrates for haemodialysis and related therapies
  • BS EN ISO 8637-1:2020 Extracorporeal systems for blood purification. Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • 22/30449721 DC BS EN ISO 23500-5. Preparation and quality management of fluids for haemodialysis and related therapies - Part 5. Quality of dialysis fluid for haemodialysis and related therapies
  • 22/30449652 DC BS EN ISO 23500-3. Preparation and quality management of fluids for haemodialysis and related therapies - Part 3. Water for haemodialysis and related therapies
  • BS EN ISO 23500-2:2019 Preparation and quality management of fluids for haemodialysis and related therapies. Water treatment equipment for haemodialysis applications and related therapies
  • BS EN ISO 8637:2014 Cardiovascular implants and extracorporeal systems. Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • BS EN 1283:1996 Haemodialysers, haemodiafilters, haemofilters, haemoconcentrators and their extracorporeal circuits
  • 23/30470631 DC BS ISO 8637-1. Extracorporeal systems for blood purification - Part 1. Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • BS EN ISO 8637-2:2024 Extracorporeal systems for blood purification - Extracorporeal blood and fluid circuits for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • BS EN ISO 8637-2:2018 Extracorporeal systems for blood purification. Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • 12/30254337 DC BS ISO 8637 AMD1. Cardiovascular implants and extracorporeal systems. Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • BS EN ISO 23118:2021 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
  • 22/30456450 DC BS EN ISO 8637-2. Extracorporeal systems for blood purification - Extracorporeal blood and fluid circuits for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • BS ISO 12771:1997 Plastics laboratory ware - Disposable serological pipettes
  • 16/30331650 DC BS EN ISO 8637-1. Extracorporeal systems for blood purification. Part 1. Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • 22/30449648 DC BS EN ISO 23500-2. Preparation and quality management of fluids for haemodialysis and related therapies - Part 2. Water treatment equipment for haemodialysis applications and related therapies
  • BS ISO 26722:2009 Water treatment equipment for haemodialysis applications and related therapies
  • BS ISO 23500:2014 Guidance for the preparation and quality management of fluids for haemodialysis and related therapies
  • BS ISO 26722:2014 Water treatment equipment for haemodialysis applications and related therapies
  • BS EN ISO 8638:2014 Cardiovascular implants and extracorporeal systems. Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters

North Atlantic Treaty Organization Standards Agency

  • STANAG 2939-2000 MEDICAL REQUIREMENTS FOR BLOOD, BLOOD DONORS AND ASSOCIATED EQUIPMENT

International Organization for Standardization (ISO)

  • ISO 13958:2014 Concentrates for haemodialysis and related therapies
  • ISO/DIS 23500-4 Preparation and quality management of fluids for haemodialysis and related therapies — Part 4: Concentrates for haemodialysis and related therapies
  • ISO 23500-4:2019 Preparation and quality management of fluids for haemodialysis and related therapies — Part 4: Concentrates for haemodialysis and related therapies
  • ISO 13959:2009 Water for haemodialysis and related therapies
  • ISO 13959:2014 Water for haemodialysis and related therapies
  • ISO/FDIS 23500-4:2011 Preparation and quality management of fluids for haemodialysis and related therapies — Part 4: Concentrates for haemodialysis and related therapies
  • ISO 23500-3:2019 Preparation and quality management of fluids for haemodialysis and related therapies — Part 3: Water for haemodialysis and related therapies
  • ISO 8638:1989 Extracorporeal blood circuit for haemodialysers, haemofilters and haemoconcentrators
  • ISO/DIS 23500-3 Preparation and quality management of fluids for haemodialysis and related therapies — Part 3: Water for haemodialysis and related therapies
  • ISO 11663:2014 Quality of dialysis fluid for haemodialysis and related therapies
  • ISO 8637:1989 Haemodialysers, haemofilters and haemoconcentrators
  • ISO/DIS 23500-5 Preparation and quality management of fluids for haemodialysis and related therapies — Part 5: Quality of dialysis fluid for haemodialysis and related therapies
  • ISO/FDIS 23500-5:2011 Preparation and quality management of fluids for haemodialysis and related therapies — Part 5: Quality of dialysis fluid for haemodialysis and related therapies
  • ISO 23500-5:2019 Preparation and quality management of fluids for haemodialysis and related therapies — Part 5: Quality of dialysis fluid for haemodialysis and related therapies
  • ISO/FDIS 8637-1:2023 Extracorporeal systems for blood purification — Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • ISO 13958:2009 Concentrates for haemodialysis and related therapies
  • ISO 13958:2002 Concentrates for haemodialysis and related therapies
  • ISO/CD 8637-1 Extracorporeal systems for blood purification — Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • ISO/DIS 8637-1 Extracorporeal systems for blood purification — Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • ISO/FDIS 8637-2:2023 Extracorporeal systems for blood purification — Part 2: Extracorporeal blood and fluid circuits for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • ISO/DIS 23500-2 Preparation and quality management of fluids for haemodialysis and related therapies — Part 2: Water treatment equipment for haemodialysis applications and related therapies
  • ISO 8637-2:2024 Extracorporeal systems for blood purification — Part 2: Extracorporeal blood and fluid circuits for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • ISO 23500-2:2019 Preparation and quality management of fluids for haemodialysis and related therapies — Part 2: Water treatment equipment for haemodialysis applications and related therapies
  • ISO 8637:2010 Cardiovascular implants and extracorporeal systems - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • ISO 8637-1:2024 Extracorporeal systems for blood purification — Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • ISO 8637-1:2017 Extracorporeal systems for blood purification - Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • ISO 8638:2004 Cardiovascular implants and artificial organs - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • ISO 8637:2004 Cardiovascular implants and artificial organs - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • ISO 8637-2:2018 Extracorporeal systems for blood purification - Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • ISO 23500-3:2024 Preparation and quality management of fluids for haemodialysis and related therapies
  • ISO 23500-4:2024 Preparation and quality management of fluids for haemodialysis and related therapies
  • ISO 8638:2010 Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • ISO/DIS 8637-2 Extracorporeal systems for blood purification — Part 2: Extracorporeal blood and fluid circuits for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • ISO 23500-5:2024 Preparation and quality management of fluids for haemodialysis and related therapies
  • ISO/TR 10686:2013 Hydraulic fluid power - Method to relate the cleanliness of a hydraulic system to the cleanliness of the components and hydraulic fluid that make up the system
  • ISO 11663:2009 Quality of dialysis fluid for haemodialysis and related therapies
  • ISO 23118:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
  • ISO 23500:2011 Guidance for the preparation and quality management of fluids for haemodialysis and related therapies
  • ISO 26722:2014 Water treatment equipment for haemodialysis applications and related therapies

Association Francaise de Normalisation

  • NF EN ISO 23500-4:2019 Preparation and quality management of hemodialysis fluids and related therapies - Part 4: concentrates for hemodialysis and related therapies
  • NF S93-305-3*NF EN ISO 23500-3:2019 Preparation and quality management of fluids for haemodialysis and related therapies - Part 3 : water for haemodialysis and related therapies
  • NF EN ISO 23500-3:2019 Preparation and quality management of hemodialysis fluids and related therapies - Part 3: water for hemodialysis and related therapies
  • NF S93-305-5*NF EN ISO 23500-5:2019 Preparation and quality management of fluids for haemodialysis and related therapies - Part 5 : quality of dialysis fluid for haemodialysis and related therapies
  • NF S93-305-4*NF EN ISO 23500-4:2019 Preparation and quality management of fluids for haemodialysis and related therapies - Part 4 : concentrates for haemodialysis and related therapies
  • NF EN ISO 23500-5:2019 Preparation and quality management of hemodialysis fluids and related therapies - Part 5: quality of dialysis fluids for hemodialysis and related therapies
  • NF S93-301:2009 Concentrates for haemodialysis and related therapies.
  • NF S93-301/IN1:2009 Concentrates for haemodialysis and related therapies.
  • NF EN ISO 8637-1:2020 Extracorporeal systems for blood purification - Part 1: hemodialyzers, hemodiafilters, hemofilters and hemoconcentrators
  • NF S93-305-2*NF EN ISO 23500-2:2019 Preparation and quality management of fluids for haemodialysis and related therapies - Part 2 : water treatment equipment for haemodialysis applications and related therapies
  • NF S93-302*NF EN ISO 8637:2014 Cardiovascular implants and extracorporeal systems - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • NF EN ISO 8637-2:2018 Extracorporeal systems for blood purification - Part 2: extracorporeal blood circuit for hemodialyzers, hemodiafilters and hemofilters
  • NF EN ISO 23500-2:2019 Preparation and quality management of fluids for hemodialysis and related therapies - Part 2: water treatment equipment for applications in hemodialysis and related therapies
  • NF S93-302-1*NF EN ISO 8637-1:2020 Extracorporeal systems for blood purification - Part 1 : haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • NF EN ISO 23118:2021 In Vitro Molecular Diagnostic Assays - Preanalytical Process Specifications for Metabolome Analysis in Urine and Venous Blood (Serum and Plasma)
  • NF S93-302-2*NF EN ISO 8637-2:2018 Extracorporeal systems for blood purification - Part 2 : extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • NF S62-084*NF EN ISO 23118:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
  • NF S93-303:2014 Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters

NATO - North Atlantic Treaty Organization

  • STANAG 2939-2010 MINIMUM REQUIREMENTS FOR BLOOD@ BLOOD DONORS AND ASSOCIATED EQUIPMENT (ED 5)

RO-ASRO

  • STAS 11326/2-1985 RUBBER STOPPERS FOR BLOOD, PLASMA AND AQUEOUS SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS Pyrogenic impurities checking up

Korean Agency for Technology and Standards (KATS)

  • KS P ISO 13959-2009(2019) Water for haemodialysis and related therapies
  • KS P ISO 13959-2021 Water for haemodialysis and related therapies
  • KS P ISO 23500-4:2021 Preparation and quality management of fluids for haemodialysis and related therapies — Part 4: Concentrates for haemodialysis and related therapies
  • KS P ISO 23500-3:2021 Preparation and quality management of fluids for haemodialysis and related therapies — Part 3: Water for haemodialysis and related therapies
  • KS B ISO 12771-2021 Plastics laboratory ware-Disposable serological pipettes
  • KS B ISO 7713-2006(2021) Laboratory glassware-Disposable serological pipettes
  • KS P 4907-2013 Haemodialysers, haemofilters and haemoconcentrators
  • KS B ISO 7713-2006(2016) Laboratory glassware-Disposable serological pipettes
  • KS P ISO 11663-2022 Quality of dialysis fluid for haemodialysis and related therapies
  • KS B ISO 12771-2006(2016) Plastics laboratory ware-Disposable serological pipettes
  • KS B ISO 12771-2006(2021) Plastics laboratory ware-Disposable serological pipettes
  • KS P ISO 8638:2012 Cardiovascular implants and extracorporeal systems -Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • KS B ISO 7713-2021 Laboratory glassware-Disposable serological pipettes
  • KS P ISO 13958:2009 Concentrates for haemodialysis and related therapies
  • KS P ISO 8637:2012 Cardiovascular implants and extracorporeal systems-Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • KS P ISO 13958-2009(2019) Concentrates for haemodialysis and related therapies
  • KS P ISO 8637-1-2023 Extracorporeal systems for blood purification — Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • KS P ISO 8638-2012(2017) Cardiovascular implants and extracorporeal systems -Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • KS P 4907-2011 Haemodialysers, haemofilters and haemoconcentrators
  • KS P ISO 13958-2021 Concentrates for haemodialysis and related therapies
  • KS P ISO 8637-2023 Cardiovascular implants and extracorporeal systems — Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • KS P ISO 8638-2022 Cardiovascular implants and extracorporeal systems -Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • KS P ISO 11663:2010 Quality of dialysis fluid for haemodialysis and related therapies
  • KS P ISO 11663:2017 Quality of dialysis fluid for haemodialysis and related therapies
  • KS P ISO 8637:2018 Cardiovascular implants and extracorporeal systems — Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators

American National Standards Institute (ANSI)

GSO

  • GSO ASTM E714:2021 Standard Specification for Disposable Glass Serological Pipets
  • GSO ISO 12771:2010 Plastics laboratory ware -- Disposable serological pipettes
  • BH GSO ISO 13959:2017 Water for haemodialysis and related therapies
  • GSO ISO 7713:2010 Laboratory glassware -- Disposable serological pipettes
  • OS GSO ISO 7713:2010 Laboratory glassware -- Disposable serological pipettes
  • GSO ISO 11663:2021 Quality of dialysis fluid for haemodialysis and related therapies
  • BH GSO ISO 11663:2022 Quality of dialysis fluid for haemodialysis and related therapies
  • OS GSO ISO 12771:2010 Plastics laboratory ware -- Disposable serological pipettes
  • ISO 23500-2:2024 Preparation and quality management of fluids for haemodialysis and related therapies — Part 2: Water treatment equipment for haemodialysis applications and related therapies
  • OS GSO ISO 8637:2016 Cardiovascular implants and extracorporeal systems -- Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • BH GSO ISO 13958:2017 Concentrates for haemodialysis and related therapies
  • GSO ISO 8637:2016 Cardiovascular implants and extracorporeal systems -- Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • OS GSO ISO 8638:2016 Cardiovascular implants and extracorporeal systems -- Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • GSO ISO 8638:2016 Cardiovascular implants and extracorporeal systems -- Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • BH GSO ISO 8637:2017 Cardiovascular implants and extracorporeal systems -- Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • GSO ISO 13958:2016 Concentrates for haemodialysis and related therapies
  • BH GSO ISO 8638:2017 Cardiovascular implants and extracorporeal systems -- Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • OS GSO ISO 13958:2016 Concentrates for haemodialysis and related therapies
  • GSO ISO 23118:2023 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
  • BH GSO ISO 23118:2023 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
  • OS GSO ISO 23500:2016 Guidance for the preparation and quality management of fluids for haemodialysis and related therapies
  • GSO ISO 23500:2016 Guidance for the preparation and quality management of fluids for haemodialysis and related therapies
  • BH GSO ASTM F2888:2023 Standard Practice for Platelet Leukocyte Count — An In-Vitro Measure for Hemocompatibility Assessment of Cardiovascular Materials
  • BH GSO ISO 23500:2017 Guidance for the preparation and quality management of fluids for haemodialysis and related therapies
  • GSO ASTM F2888:2023 Standard Practice for Platelet Leukocyte Count — An In-Vitro Measure for Hemocompatibility Assessment of Cardiovascular Materials

ES-UNE

  • UNE-EN ISO 23500-4:2019 Preparation and quality management of fluids for haemodialysis and related therapies - Part 4: Concentrates for haemodialysis and related therapies (ISO 23500-4:2019)
  • ISO/FDIS 23500-3:2023 Preparation and quality management of fluids for haemodialysis and related therapies — Part 3: Water for haemodialysis and related therapies
  • UNE-EN ISO 23500-3:2019 Preparation and quality management of fluids for haemodialysis and related therapies - Part 3: Water for haemodialysis and related therapies (ISO 23500-3:2019)
  • UNE-EN ISO 23500-5:2019 Preparation and quality management of fluids for haemodialysis and related therapies - Part 5: Quality of dialysis fluid for haemodialysis and related therapies (ISO 23500-5:2019)
  • UNE-EN ISO 8637-1:2020 Extracorporeal systems for blood purification - Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637-1:2017)
  • UNE-EN ISO 23500-2:2019 Preparation and quality management of fluids for haemodialysis and related therapies - Part 2: Water treatment equipment for haemodialysis applications and related therapies (ISO 23500-2:2019)
  • ISO/FDIS 23500-2:2023 Preparation and quality management of fluids for haemodialysis and related therapies — Part 2: Water treatment equipment for haemodialysis applications and related therapies
  • UNE-EN ISO 8637-2:2019 Extracorporeal systems for blood purification - Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (ISO 8637-2:2018)
  • UNE-EN ISO 23118:2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO 23118:2021)

KR-KS

  • KS P ISO 23500-3-2021 Preparation and quality management of fluids for haemodialysis and related therapies — Part 3: Water for haemodialysis and related therapies
  • KS P ISO 23500-4-2021 Preparation and quality management of fluids for haemodialysis and related therapies — Part 4: Concentrates for haemodialysis and related therapies
  • KS P ISO 11663-2017 Quality of dialysis fluid for haemodialysis and related therapies
  • KS P ISO 8637-2-2022 Extracorporeal systems for blood purification — Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • KS P ISO 8637-2018 Cardiovascular implants and extracorporeal systems — Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • KS P ISO 23500-5-2022 Preparation and quality management of fluids for haemodialysis and related therapies — Part 5: Quality of dialysis fluid for haemodialysis and related therapies

German Institute for Standardization

  • DIN EN ISO 23500-4:2022-12 Preparation and quality management of fluids for haemodialysis and related therapies - Part 4: Concentrates for haemodialysis and related therapies (ISO/DIS 23500-4:2022); German and English version prEN ISO 23500-4:2022 / Note: Date of issue 2022-11-1...
  • DIN EN ISO 23500-4:2019-11 Preparation and quality management of fluids for haemodialysis and related therapies - Part 4: Concentrates for haemodialysis and related therapies (ISO 23500-4:2019); German version EN ISO 23500-4:2019 / Note: To be replaced by DIN EN ISO 23500-4 (202...
  • DIN EN ISO 23500-3:2019-11 Preparation and quality management of fluids for haemodialysis and related therapies - Part 3: Water for haemodialysis and related therapies (ISO 23500-3:2019); German version EN ISO 23500-3:2019 / Note: To be replaced by DIN EN ISO 23500-3 (2022-12).
  • DIN EN ISO 23500-3:2022-12 Preparation and quality management of fluids for haemodialysis and related therapies - Part 3: Water for haemodialysis and related therapies (ISO/DIS 23500-3:2022); German and English version prEN ISO 23500-3:2022 / Note: Date of issue 2022-11-18*Inten...
  • DIN EN ISO 23500-5:2019-11 Preparation and quality management of fluids for haemodialysis and related therapies - Part 5: Quality of dialysis fluid for haemodialysis and related therapies (ISO 23500-5:2019); German version EN ISO 23500-5:2019 / Note: To be replaced by DIN EN ISO...
  • DIN EN ISO 23500-5:2022-12 Preparation and quality management of fluids for haemodialysis and related therapies - Part 5: Quality of dialysis fluid for haemodialysis and related therapies (ISO/DIS 23500-5:2022); German and English version prEN ISO 23500-5:2022 / Note: Date of is...
  • DIN EN ISO 23500-4:2019 Preparation and quality management of fluids for haemodialysis and related therapies - Part 4: Concentrates for haemodialysis and related therapies (ISO 23500-4:2019)
  • DIN EN ISO 8637-1:2020-10 Extracorporeal systems for blood purification - Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637-1:2017); German version EN ISO 8637-1:2020
  • DIN EN ISO 23500-3:2019 Preparation and quality management of fluids for haemodialysis and related therapies - Part 3: Water for haemodialysis and related therapies (ISO 23500-3:2019)
  • DIN EN ISO 23500-2:2022-12 Preparation and quality management of fluids for haemodialysis and related therapies - Part 2: Water treatment equipment for haemodialysis applications and related therapies (ISO/DIS 23500-2:2022); German and English version prEN ISO 23500-2:2022 / Not...
  • DIN EN ISO 13959:2016 Water for haemodialysis and related therapies (ISO 13959:2014)
  • DIN EN ISO 23500-2:2019-11 Preparation and quality management of fluids for haemodialysis and related therapies - Part 2: Water treatment equipment for haemodialysis applications and related therapies (ISO 23500-2:2019); German version EN ISO 23500-2:2019 / Note: To be replaced ...
  • DIN EN ISO 23500-5:2019 Preparation and quality management of fluids for haemodialysis and related therapies - Part 5: Quality of dialysis fluid for haemodialysis and related therapies (ISO 23500-5:2019)
  • DIN EN ISO 23500-4:2017 Guidance for the preparation and quality management of fluids for haemodialysis and related therapies - Part 4: Concentrates for haemodialysis and related therapies (ISO/DIS 23500-4:2017); German and English version prEN ISO 23500-4:2017
  • DIN EN ISO 8637-2:2018-12 Extracorporeal systems for blood purification - Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (ISO 8637-2:2018); German version EN ISO 8637-2:2018 / Note: To be replaced by DIN EN ISO 8637-2 (2023-01).
  • DIN EN ISO 23500-3:2017 Guidance for the preparation and quality management of fluids for haemodialysis and related therapies - Part 3: Water for haemodialysis and related therapies (ISO/DIS 23500-3:2017); German and English version prEN ISO 23500-3:2017
  • DIN EN ISO 8637-2:2023-01 Extracorporeal systems for blood purification - Part 2: Extracorporeal blood and fluid circuits for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO/DIS 8637-2:2022); German and English version prEN ISO 8637-2:2022 / Note: Date...
  • DIN 58934-1:1997 Haematology - Control material for the CBC - Part 1: Control bloods
  • DIN 12750:1969 Blood dilution pipettes for blood corpuscles counting
  • DIN EN ISO 23500-5:2017 Guidance for the preparation and quality management of fluids for haemodialysis and related therapies - Part 5: Quality of dialysis fluid for haemodialysis and related therapies (ISO/DIS 23500-5:2017); German and English version prEN ISO 23500-5:2017
  • DIN EN ISO 23500-2:2019 Preparation and quality management of fluids for haemodialysis and related therapies - Part 2: Water treatment equipment for haemodialysis applications and related therapies (ISO 23500-2:2019)
  • DIN EN ISO 23118:2021-08 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO 23118:2021); German version EN ISO 23118:2021
  • DIN 58931:1995 Haematology - Determination of haemoglobin concentration in blood - Reference method
  • DIN EN ISO 8637-1:2020 Extracorporeal systems for blood purification - Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637-1:2017)
  • DIN 58931:2021-09 Haematology - Determination of haemoglobin concentration in blood - Reference method; Text in German and English
  • DIN 58931:2021 Haematology - Determination of haemoglobin concentration in blood - Reference method; Text in German and English
  • DIN 12750:1969-02 Blood dilution pipettes for blood corpuscles counting
  • DIN EN ISO 13958:2016 Concentrates for haemodialysis and related therapies (ISO 13958:2014)

US-AAMI

  • ANSI/AAMI 13959-2014 Water for hemodialysis and related therapies
  • ANSI/AAMI 11663-2014 Quality of dialysis fluid for haemodialysis and related therapies
  • ANSI/AAMI/ISO 8637:2010 Cardiovascular implants and extracorporeal systems - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • ANSI/AAMI RD16-2007 Cardiovascular implants and artificial organs-Hemodialyzers,hemodiafilters,hemofilters,and hemoconcentrators
  • ANSI/AAMI 13958-2014 Concentrates for hemodialysis and related therapies
  • ANSI/AAMI RD17-2007 Cardiovascular implants and artificial organs - Extracorporeal blood circuit for hemodialyzers, hemodiafilters and hemofilters
  • AAMI 23500-2014 Guidance for the preparation and quality management of fluids for hemodialysis and related therapies

ES-AENOR

American Society for Testing and Materials (ASTM)

RU-GOST R

  • GOST 27422-1987 Apparatus for nonkidney blood treatment. General specifications
  • GOST 33674-2015 Blood and processed products. Specifications
  • GOST R 53470-2009 Blood and blood components. Management on application of components of donor blood
  • GOST R ISO 13958-2015 Concentrates for haemodialysis and related therapies
  • GOST R 52938-2008 Blood and blood components. Containers with blood or blood components. Labeling
  • GOST R ISO 8638-1999 Extracorporeal blood circuit for haemodialysers, haemofilters and haemoconcentrators. Technical requirements and test methods
  • GOST 16445-2012 Serum haemolitic for the complement fixation test. Specification
  • GOST ISO 8638-2012 Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemoconcentrators. Technical requirements and test methods
  • GOST ISO 8637-2012 Haemodialysers, haemofiltres and haemoconcentrators. Technical requirements and test methods

CEN - European Committee for Standardization

  • EN ISO 23500-4:2019 Preparation and quality management of fluids for haemodialysis and related therapies - Part 4: Concentrates for haemodialysis and related therapies
  • EN ISO 23500-3:2019 Preparation and quality management of fluids for haemodialysis and related therapies - Part 3: Water for haemodialysis and related therapies
  • EN ISO 23500-5:2019 Preparation and quality management of f luids for haemodialysis and related therapies - Part 5: Quality of dialysis f luid for haemodialysis and related therapies
  • EN ISO 23500-2:2019 Preparation and quality management of fluids for haemodialysis and related therapies - Part 2: Water treatment equipment for haemodialysis applications and related therapies
  • EN ISO 8637-2:2018 Extracorporeal systems for blood purification - Part 2: Extracorporeal blood circuit for haemodialysers@ haemodiafilters and haemofilters

Canadian Standards Association (CSA)

  • CAN/CSA-ISO 13958:2015 Concentrates for haemodialysis and related therapies (Second Edition)
  • CAN/CSA-ISO 11663:2015 Quality of dialysis fluid for haemodialysis and related therapies (Second Edition)
  • CAN/CSA-ISO 13959:2015 Water for haemodialysis and related therapies (Second Edition)
  • CAN/CSA-ISO 13959:2011 Eau pour hémodialyse et thérapies apparentées (Première Édition)
  • CSA Z8637-08-CAN/CSA-2008 Cardiovascular implants and artificial organs ?Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • CAN/CSA-ISO 8637:2012 Cardiovascular implants and extracorporeal systems — Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (First Edition)
  • CAN/CSA-ISO 8638:2013 Implants cardiovasculaires et systèmes extracorporels - Circuit sanguin extracorporel pour les hémodialyseurs, les hémodiafiltres et les hémofiltres (première édition)
  • CAN/CSA-ISO 8638:2012 Cardiovascular implants and extracorporeal systems — Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (First Edition)
  • CSA Z902-04-CAN/CSA-2004 Sang et produits sanguins labiles Premiere Edition
  • CSA Z364.1.1/Z364.1.2-94-1994 Hemodialyseurs, Hemofiltres Et Hemoconcentrateurs Deuxieme Edition; Fiche No 1
  • CSA ISO 8637-1:2021 Extracorporeal systems for blood purification - Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (Adopted ISO 8637-1:2017, first edition, 2017-11)

Military Standards (MIL-STD)

Japanese Industrial Standards Committee (JISC)

  • JIS T 3250:2022 Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • JIS T 3250:2005 Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • JIS T 3250:2011 Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • JIS T 3250:2013 Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators

European Committee for Standardization (CEN)

  • EN ISO 8637:2014 Cardiovascular implants and extracorporeal systems - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637:2010, including Amendment 1 2013-04-01)
  • FprEN ISO 23500-4 Preparation and quality management of fluids for haemodialysis and related therapies - Part 4: Concentrates for haemodialysis and related therapies (ISO/FDIS 23500-4:2024)
  • prEN ISO 23500-4 Preparation and quality management of fluids for haemodialysis and related therapies - Part 4: Concentrates for haemodialysis and related therapies (ISO/DIS 23500-4:2022)
  • FprEN ISO 23500-3 Preparation and quality management of fluids for haemodialysis and related therapies - Part 3: Water for haemodialysis and related therapies (ISO/FDIS 23500-3:2024)
  • prEN ISO 23500-3 Preparation and quality management of fluids for haemodialysis and related therapies - Part 3: Water for haemodialysis and related therapies (ISO/DIS 23500-3:2022)
  • FprEN ISO 23500-5 Preparation and quality management of fluids for haemodialysis and related therapies - Part 5: Quality of dialysis fluid for haemodialysis and related therapies (ISO/FDIS 23500-5:2024)
  • prEN ISO 23500-5 Preparation and quality management of fluids for haemodialysis and related therapies - Part 5: Quality of dialysis fluid for haemodialysis and related therapies (ISO/DIS 23500-5:2022)
  • EN ISO 8637-1:2020 Extracorporeal systems for blood purification - Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637-1:2017)
  • FprEN ISO 8637-2 Extracorporeal systems for blood purification - Part 2: Extracorporeal blood and fluid circuits for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO/FDIS 8637-2:2023)
  • EN 1283:1996 Haemodialysers, Haemodiafilters, Haemofilters, Haemoconcentrators and Their Extracorporeal Circuits
  • EN ISO 8638:2014 Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers@ haemodiafilters and haemofilters
  • prEN ISO 23500-2 Preparation and quality management of fluids for haemodialysis and related therapies - Part 2: Water treatment equipment for haemodialysis applications and related therapies (ISO/DIS 23500-2:2022)
  • EN ISO 23118:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO 23118:2021)
  • prEN ISO 8637-2 Extracorporeal systems for blood purification - Part 2: Extracorporeal blood and fluid circuits for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO/DIS 8637-2:2022)

US-FCR

Danish Standards Foundation

  • DS/EN ISO 8637-1:2021 Extracorporeal systems for blood purification – Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • DS/EN 1283:1997 Haemodialysers, haemodiafilters, haemofilters, haemoconcentrators and their extracorporeal circuits
  • DS/EN 13867+A1:2009 Concentrates for haemodialysis and related therapies
  • DS/ISO 23118:2021 Molecular in vitro diagnostic examinations – Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma

CZ-CSN

Lithuanian Standards Office

Indonesia Standards

  • SNI ISO 8638:2012 Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters

AT-ON

  • ONORM EN 1283-1996 Haemodialysers,haemodiafilters,haemofilters,haemoconcentrators and their extracorporeal circuits

DIN

SE-SIS

IT-UNI

  • UNI EN ISO 23118:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma

AENOR

  • UNE-EN ISO 8638:2014 Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (ISO 8638:2010)

YU-JUS

  • JUS B.E4.095-1981 Bottles for conservated human blood, derivate of blood, parenteral solution and water for injections

HU-MSZT