plasma whole blood
plasma whole blood, Total:82 items.
The international standard classification for "plasma whole blood" includes: Medical Sciences and health care facilities in general , Surgical instruments and materials , Transfusion, infusion and injection equipment , Implants for surgery, prosthetics and orthotics , Health care technology (Vocabularies) .
The Chinese standard classification for "plasma whole blood" includes: Medical science , Health quarantine , Extracorporeal circulation, artificial organ and prosthesis device , General and microsurgical devices , Sanitation in general .
未注明发布机构
- 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 58903 E:2019-04 Haemostaseology - Deficient plasma - Requirements, preparation
- DIN 58905-1 E:2015-12 Haemostaseology - Blood collection - Part 1: Preparation of plasma from citrated venous blood for coagulation testing
国家市场监督管理总局、中国国家标准化管理委员会
- GB/T 38576-2020 Collection and processing of human blood biomaterial
Fujian Provincial Standard of the People's Republic of China
- DB35/T 74-1996 Methods for determination of blood concentrations of antiepileptic drugs
卫生健康委员会
- WS/T 623-2018 Transfusion of whole blood and blood components
Professional Standard - Commodity Inspection
- SN/T 1608-2005 Codes for preservation and management of blood specimens in clinical laboratories at frontier port
Group Standards of the People's Republic of China
- T/CSBME 023-2020 Plasma thawing device
- T/CSBME 022-2020 Plasma quick-freezer
- T/CSBME 057-2022 Adsorption resin for hemoperfusion or plasma perfusion devices
- T/TSSP 013-2022 Sansui Plasma Duck
- T/NBPIA 001-2020 Specifications for blood purification facility configuration
Professional Standard - Medicine
- YY 0053-2016 Hemodialysis and relavant therapics -Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
- YY 0326.1-2002 Plasmapheresis centrifuge appararus for single use - Part 1: Centrifuge bowl
- YY 0326.2-2002 Plasmapheresis centrifuge appararus for single use--Part 2:Plasma tubing
- YY 0326.3-2005 Plasmapheresis centrifuge apparatus for single use-
- YY/T 1510-2017 Medical plasma virus inactivated device
- YY/T 1902-2024 Medical plasma quick freezer
Tianjin Provincial Standard of the People's Republic of China
- DB12/T 751-2017 Specifications for the construction of blood transfusion departments (blood banks) in medical institutions
Professional Standard - Agriculture
- 627药典 化学药和生物制品卷-2010 Chapter VIII Drugs for Blood System Section IV Plasma Substitute Gelatin
- 20药典 三部-2020 General principles of biological products Human plasma for the manufacture of blood products
- 8药典 三部-2010 General headings Human plasma for the production of blood products
- 790药典 中药成方制剂卷-2010 Sections on Internal Medicine 15. Blood Regulating Agents (7) Hemostasis Sedum Notoginseng Syrup
- 23药典 三部-2015 General principles of biological products Human plasma for the manufacture of blood products
- 1167药典 中药成方制剂卷-2010 Each Discussion on Gynecology 1. Menstruation Regulating Agent (4) Angelica Syrup for Nourishing Qi and Blood
国家药监局
- YY 0465-2019 Disposable membrane plasmaseparator and plasma component separator
Professional Standard - Hygiene
- WS/T 359-2011 Collection and processing of blood specimens for testing plasma-based coagulation assays
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
General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China
- GB 18469-2012 Quality requirements for whole blood and blood components
- GB 18469-2001 STANDARDs for whole blood and blood components quality
中华人民共和国国家卫生和计划生育委员会
- WS/T 122-1999 Quantitative determination of hemoglobin in whole blood
国家卫生计生委
- WS/T 550-2017 Guidelines for quality monitoring of whole blood and blood components
SCC
- AENOR UNE 23052:1971 BLOOD TRANSFUSION. DRIED HUMAN BLOOD PLASMA
- AENOR UNE 23051:1971 BLOOD TRANSFUSION. LIQUID HUMAN BLOOD PLASMA
- DIN 58903 E:2019 Draft Document - Haemostaseology - Deficient plasma - Requirements, preparation; Text in German and English
- 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
- 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
- DANSK DS/CEN/TS 17742:2022 Molecular in vitro diagnostic examinations – Specifications for pre-examination processes for venous whole blood – Isolated circulating cell free RNA from plasma
German Institute for Standardization
- DIN 58903:2000 Haemostaseology - Deficient plasma - Requirements, preparation
- DIN 58905-1:2000 Haemostaseology - Blood collection - Part 1: Preparation of plasma from citrated venous blood for coagulation testing
- DIN 58903:2020 Haemostaseology - Deficient plasma - Requirements, preparation; Text in German and English
- DIN 58903:2020-04 Haemostaseology - Deficient plasma - Requirements, preparation; 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 1326-1:1991-10 Plasmas; physical principles
- DIN 58905-1:2016-12 Haemostaseology - Blood collection - Part 1: Preparation of plasma from citrated venous blood for coagulation testing; Text in German and English
- DIN 58930:2002-08 Haemostaseology - INR calibration plasmas - Requirements, preparation and use
- DIN 58939-1:2000-03 Haemostaseology - Reference plasma - Part 1: Requirements, preparation
- DIN 58939-1:2000 Haemostaseology - Reference plasma - Part 1: Requirements, preparation
- DIN 58930:2002 Haemostaseology - INR calibration plasmas - Requirements, preparation and use
- 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 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 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
Military Standards (MIL-STD)
- DOD A-A-51826-1987 SEPARATOR, SERUM AND PLASMA
- DOD A-A-55711-1996 FREEZER, UNDER COUNTER, BLOOD PLASMA
- DOD A-A-50812 A-1989 PIPET, BLOOD DILUTING
CZ-CSN
- CSN ON 85 6263-1964 Plastic blood transfusion system for dry plasma transfusion
- CSN 86 4810-1964 Human Dried Plasma
British Standards Institution (BSI)
- BS ISO 8637-3:2024 Extracorporeal systems for blood purification - Plasmafilters
- BS EN ISO 20186-3:2019 Molecular in-vitro diagnostic examinations. Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free DNA from plasma
- BS 4376-2:1996 Electrically operated blood storage refrigerators - Specification for cabinets for the storage of frozen plasma
RO-ASRO
- STAS 5442-1987 RUBBER STOPPERS FOR BLOOD, PLASMA AND AQUEOUS PERFUSABLE SOLUTION VIALS
- STAS 5327-1978 SCREW THREAD FOR GLASS BOTTLES FOR BLOOD AND PLASMA
- STAS 5329-1989 GLASS BOTTLES FOR PLASMA
- STAS 11326/6-1985 RUBBER STOPPERS FOR BLOOD, PLASMA AND A QUEOUS SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS Inocuity checking up
- STAS 11326/3-1984 RUBBER STOPPERS FOR INJECTABLE AND PERFUSABLE BLOOD, PLASMA AND AQUEOUS SOLUTION BOTTLES Toxicity checking up
- STAS 11327/3-1983 RUBBER STOPPERS FOR BLOOD,PLASMA AND SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS pH aqueous extract checking out
- STAS 11326/8-1985 RUBBER STOPPERS FOR BLOOD, PLASMA AND INJECTABLE AND PERFUSABLE AQUEOUS SOLUTIONS Microbiological checking up of poisonous substances with antibacterian action
- STAS 11326/2-1985 RUBBER STOPPERS FOR BLOOD, PLASMA AND AQUEOUS SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS Pyrogenic impurities checking up
RU-GOST R
- GOST 16445-1978 Haemolytic serum for the compliment fixation test. Specifications
GSO
- GSO ISO 13960:2015 Cardiovascular implants and extracorporeal systems -- Plasmafilters
Korean Agency for Technology and Standards (KATS)
- KS P ISO 13960:2017 Cardiovascular implants and extracorporeal systems — Plasmafilters
- KS P ISO 13960:2010 Cardiovascular implants and artificial organs-Plasmafilters
International Organization for Standardization (ISO)
- ISO 13960:2003 Cardiovascular implants and artificial organs - Plasmafilters
- ISO 13960:2010 Cardiovascular implants and extracorporeal systems - Plasmafilters
- ISO 8637-3:2018 Extracorporeal systems for blood purification - Part 3: Plasmafilters
- ISO 8637-3:2024 Extracorporeal systems for blood purification — Part 3: Plasmafilters
KR-KS
- KS P ISO 8637-3-2022 Extracorporeal systems for blood purification Part 3: Plasmafilters
European Committee for Standardization (CEN)
- FprCEN/TS 17742-2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma
- CEN/TS 17742:2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma
ES-UNE
- UNE-CEN/TS 17742:2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma (Endorsed by Asociación Española de Normalización in May of 2022.)
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