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  1. HOME
  2. Standards for The relationship between blood coagulation and blood draw volume

The relationship between blood coagulation and blood draw volume

The relationship between blood coagulation and blood draw volume, Total:155 items.

The international standard classification for "The relationship between blood coagulation and blood draw volume" includes: Medical Sciences and health care facilities in general , Surgical instruments and materials , Laboratory medicine .

The Chinese standard classification for "The relationship between blood coagulation and blood draw volume" includes: Sanitation in general , Extracorporeal circulation, artificial organ and prosthesis device , Medical laboratory equipment .

Professional Standard - Agriculture

未注明发布机构

  • DIN 58909-2 E:2019-04 Haemostaseology - Determination of factor VIII coagulant activity (FVIII:C) - Part 2: Reference measurement procedure using a synthetic peptide substrate
  • DIN EN 1283:1996 Hemodialyzers, hemodiafilters, hemofilters, hemoconcentrators and associated LJ blood tubing systems
  • ANSI/AAMI/ISO 8637-2:2018 Extracorporeal systems for blood purification— Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • DIN 58909-1 E:2018-09 Haemostaseology - Determination of factor VIII coagulant activity (F VIII C) - Part 1: Reference measurement procedure for the one-stage method
  • CSA ISO 8637-2:2021 Extracorporeal systems for blood purification — Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • DIN 58910-1 E:2014-12 Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 1: Reference measurement procedure for the determination in plasma from citrated venous blood
  • CLSI H21-2024 Collection, Transport, and Processing of Blood Specimens for Testing Plasma-Based Coagulation Assays
  • DIN 58908 E:2014-12 Haemostaseology - Determination of activated partial thromboplastin time (APTT) - Reference measurement procedure
  • DIN 58905-1 E:2015-12 Haemostaseology - Blood collection - Part 1: Preparation of plasma from citrated venous blood for coagulation testing
  • DIN EN ISO 8638 E:2013-06 Cardiovascular implants and extracorporeal systems Hemodialyzers, hemodiafilters and hemofilters for extracorporeal circulation (draft)

Professional Standard - Hygiene

  • WS/T 359-2011 Collection and processing of blood specimens for testing plasma-based coagulation assays
  • WS/T 359-2024 Specimen collection and processing for common items of thrombosis and hemostasis testing

Professional Standard - Medicine

  • YY 0267-2016 Hemodialysis and related therapies―Extracorporeal blood circuit for blood purification devices

National Health Commission of the People's Republic of China

  • WST 359:2011 Guidelines for the Collection and Processing of Blood Specimens for Plasma Coagulation Tests

Zhejiang Provincial Standard of the People's Republic of China

  • DB33/T 918.6-2021 Blood Information System Basic Construction Specification Part 6: Basic Data Set for Information Sharing between Blood Stations and Plasmapheresis Stations

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）

German Institute for Standardization

  • DIN 58910-4:2000-03 Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 4: Reference measurement procedure for the determination in capillary blood
  • DIN 58910-1:2016-02 Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 1: Reference measurement procedure for the determination in plasma from citrated venous blood; Text in German and English
  • DIN 58910-3:2000-03 Haemostaseology - Determination of the thromboplastin (prothrombin) time - Part 3: Reference measurement procedure for the determination in citrated capillary blood
  • DIN 58909-1:2000 Haemostaseology - Determination of factor VIII coagulant activity (F VIII C) - Part 1: Reference measurement procedure for the one-stage method
  • DIN 58902:2000 Haemostaseology - Reference measurement procedure for the determination of batroxobin time
  • DIN 58910-2:2000-03 Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 2: Reference measurement procedure for the determination in citrated venous blood
  • DIN 58914-1:2000-03 Haemostaseology - Determination of thrombin time - Part 1: Reference measurement procedure for the determination in plasma from citrated venous blood
  • DIN 58911-1:2000-03 Haemostaseology - Calibration of measurement procedures - Part 1: Clotting time measurement procedures
  • DIN 58909-2:2000 Haemostaseology - Determination of factor VIII coagulant activity (F VIII C) - Part 2: Reference measurement procedure using a synthetic peptide substrate
  • DIN 58905-1:2000 Haemostaseology - Blood collection - Part 1: Preparation of plasma from citrated venous blood for coagulation testing
  • DIN 58913-1:2000 Haemostaseology - Determination of factor II coagulant activity (F II C) and factor X coagulant activity (F X C) - Part 1: Reference measurement procedure for the one-stage method
  • DIN 58907-1:2000 Haemostaseology - Determination of factor IX coagulant activity (F IX C) - Part 1: Reference measurement procedure for the one-stage method
  • DIN 58914-1:2000 Haemostaseology - Determination of thrombin time - Part 1: Reference measurement procedure for the determination in plasma from citrated venous blood
  • DIN 58910-1:2000 Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 1: Reference measurement procedure for the determination in plasma from citrated venous blood
  • DIN 58910-1:2016 Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 1: Reference measurement procedure for the determination in plasma from citrated venous blood; Text in German and English
  • DIN 58913-1:2000-03 Haemostaseology - Determination of factor II coagulant activity (F II C) and factor X coagulant activity (F X C) - Part 1: Reference measurement procedure for the one-stage method
  • DIN 58910-4:2000 Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 4: Reference measurement procedure for the determination in capillary blood
  • DIN 58908:2015-09 Haemostaseology - Determination of activated partial thromboplastin time (APTT) - Reference measurement procedure; Text in German and English
  • DIN 58905-1:2016 Haemostaseology - Blood collection - Part 1: Preparation of plasma from citrated venous blood for coagulation testing; Text in German and English
  • DIN 58911-1:2000 Haemostaseology - Calibration of measurement procedures - Part 1: Clotting time measurement procedures
  • DIN 58910-2:2000 Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 2: Reference measurement procedure for the determination in citrated venous blood
  • DIN 58909-2:2020 Haemostaseology - Determination of factor VIII coagulant activity (FVIII:C) - Part 2: Reference measurement procedure using a synthetic peptide substrate; Text in German and English
  • DIN 58910-3:2000 Haemostaseology - Determination of the thromboplastin (prothrombin) time - Part 3: Reference measurement procedure for the determination in citrated capillary blood
  • DIN 58908:2000 Haemostaseology - Determination of activated partial thromboplastin time (APTT) - Reference measurement procedure
  • DIN 58909-1:2020-04 Haemostaseology - Determination of factor VIII coagulant activity (FVIII:C) - Part 1: Reference measurement procedure for the one-stage method; Text in German and English
  • DIN 58909-1:2020 Haemostaseology - Determination of factor VIII coagulant activity (FVIII:C) - Part 1: Reference measurement procedure for the one-stage method; Text in German and English
  • DIN 58907-1:2000-03 Haemostaseology - Determination of factor IX coagulant activity (F IX C) - Part 1: Reference measurement procedure for the one-stage method
  • DIN 58901-1:2000-03 Haemostaseology - Determination of factor VII coagulant activity (F VII C) - Part 1: Reference measurement procedure for the one-stage method

SCC

  • AWWA JAW63326 Journal AWWA — An Evaluation of the Relationship between SUVA and NOM Coagulation Using the ICR Database
  • DIN 58910-1 E:2014 Draft Document - Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 1: Reference measurement procedure for the determination in plasma from citrated venous blood; Text in German and English
  • AWWA QTC97026 The Role of Coagulation in DBP-Related Risk Reduction
  • AWWA ACE60048 Stoichiometry of Coagulation Revisited
  • DIN 58908 E:2014 Draft Document - Haemostaseology - Determination of activated partial thromboplastin time (APTT) - Reference measurement procedure; Text in German and English
  • AWWA ACE56186 Coagulation Changes for Future Regulations
  • BS 7297-2:1990 Haemodialysers and related equipment-Specification for extracorporeal circuits for use with haemodialysers, haemofilters and haemoconcentrators
  • AWWA QTC98332 Assessing the Secondary Impacts of Enhanced Coagulation
  • AS 3787.2:1992 General requirements for single-use, sterile, plasticized polyvinyl chloride (PVC) blood packs for whole blood and blood components - Multiple blood pack systems
  • NS-EN 1060-3:1997 Non-invasive sphygmomanometers — Part 3: Supplementary requirements for electro-mechanical blood pressure measuring systems

RU-GOST R

  • GOST R 53470-2009 Blood and blood components. Management on application of components of donor blood
  • GOST R ISO 8638-1999 Extracorporeal blood circuit for haemodialysers, haemofilters and haemoconcentrators. Technical requirements and test methods
  • GOST R 53420-2009 Blood and blood components. General requirements for quality assurance of collection, processing and use of blood and blood components

CZ-CSN

ES-AENOR

North Atlantic Treaty Organization Standards Agency

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

Association Francaise de Normalisation

  • NF S97-531:2002 Medical informatics - Messages concerning blood transfusion - Nominative delivery message and report on nominative delivery message.
  • NF U47-210:2009 Isolation of hemagglutinating avian myxoviruses by ovoculture and detection of their hemagglutinating activity.
  • NF EN 1060-3/IN2:2010 Non-invasive blood pressure monitors - Part 3: additional requirements for electromechanical blood pressure measurement systems
  • NF EN ISO 8637-2:2018 Extracorporeal systems for blood purification - Part 2: extracorporeal blood circuit for hemodialyzers, hemodiafilters and hemofilters
  • NF S93-303:2014 Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters

API - American Petroleum Institute

  • API PUBL 27-30700- STUDIES ON THE EVALUATION OF PROBLEMS ASSOCIATED WITH THE MEASUREMENT OF LOW CONCENTRATIONS OF CARBOXYHEMOGLOBIN

Military Standards (MIL-STD)

NATO - North Atlantic Treaty Organization

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

Korean Agency for Technology and Standards (KATS)

  • KS P ISO 8638-2012(2017) Cardiovascular implants and extracorporeal systems －Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • KS P ISO 8638-2022 Cardiovascular implants and extracorporeal systems －Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters

Standard Association of Australia （SAA）

  • AS EN 1060.3:2004 Non-invasive sphygmomanometers - Supplementary requirements for electromechanical blood pressure measuring systems

British Standards Institution (BSI)

  • BS EN ISO 8637-1:2020 Extracorporeal systems for blood purification. Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • BS DD ENV 13730-2:2002 Healthcare informatics - Blood transfusion related messages - Production related messages (BTR-PROD)
  • 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 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 8637-2:2018 Extracorporeal systems for blood purification. Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • BS EN ISO 23500-4:2024 Preparation and quality management of fluids for haemodialysis and related therapies - Concentrates 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 EN ISO 8637-2:2024 Extracorporeal systems for blood purification - Extracorporeal blood and fluid circuits for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • BS EN ISO 8638:2014 Cardiovascular implants and extracorporeal systems. Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters

Indonesia Standards

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

GSO

  • 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 8638:2017 Cardiovascular implants and extracorporeal systems -- Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters

European Committee for Standardization (CEN)

  • EN ISO 23500:2015 Guidance for the preparation and quality management of fluids for haemodialysis and related therapies

American National Standards Institute （ANSI)

American Society for Testing and Materials (ASTM)

Lithuanian Standards Office

  • LST EN 1060-3-2000+A2-2010 Non-invasive sphygmomanometers - Part 3: Supplementary requirements for electro-mechanical blood pressure measuring systems

International Organization for Standardization (ISO)

  • ISO 8638:2010 Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters

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