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DEvenous whole blood venous plasma
venous whole blood venous plasma, Total:149 items.
In the international standard classification, venous whole blood venous plasma involves: Medical sciences and health care facilities in general, Precision mechanics, Laboratory medicine, Veterinary medicine, Materials for aerospace construction, Medical equipment, Farming and forestry, Pharmaceutics, Construction materials.
Group Standards of the People's Republic of China, venous whole blood venous plasma
Military Standards (MIL-STD), venous whole blood venous plasma
未注明發(fā)布機構, venous whole blood venous plasma
- DIN 58905-1 E:2015-12 Haemostaseology - Blood collection - Part 1: Preparation of plasma from citrated venous blood for coagulation testing
- 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
- ANSI/AAMI/ISO 25539-3:2011(2015) Cardiovascular implants — Endovascular devices — Part 3: Vena cava filters
- DIN EN ISO 6710 E:2016-11 Disposable containers for human venous blood sample collection (draft)
- DIN EN ISO 20186-3 E:2018-02 Procedure Specification for Preliminary Examination of Venous Whole Blood for Molecular In Vitro Diagnostic Examination Part 3: Isolation of Circulating Cell-Free DNA from Plasma (Draft)
German Institute for Standardization, venous whole blood venous plasma
- DIN 58905-1:2000 Haemostaseology - Blood collection - Part 1: Preparation of plasma from citrated venous blood for coagulation testing
- 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 58905-1:2016 Haemostaseology - Blood collection - Part 1: Preparation of plasma from citrated venous blood for coagulation testing; Text in German and English
- 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 CEN/TS 17742:2022-07 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma; German version CEN/TS 17742:2022
- 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 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 EN 14820:2004 Single-use containers for human venous blood specimen collection; German version EN 14820:2004
- DIN EN ISO 25539-3:2012-03 Cardiovascular implants - Endovascular devices - Part 3: Vena cava filters (ISO 25539-3:2011); German version EN ISO 25539-3:2011
- DIN 58914-1:2000 Haemostaseology - Determination of thrombin time - Part 1: Reference measurement procedure for the determination in plasma from citrated venous blood
- DIN 58910-1:2016 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 58910-1:2000 Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 1: Reference measurement procedure for the determination in plasma from citrated venous blood
- DIN EN ISO 20186-3:2020-04 Molecular in-vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasma (ISO 20186-3:2019); German version EN ISO 20186-3:2019
- DIN EN ISO 23118:2020 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO/DIS 23118:2020); German and English version prEN ISO 23118:2020
- DIN EN ISO 20186-3:2020 Molecular in-vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasma (ISO 20186-3:2019)
SCC, venous whole blood venous plasma
- AS 2636:1983 Sampling of venous and capillary blood for the determination of lead content
- 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
- BS ISO 6710:1995 Single-use containers for venous blood specimen collection
- AS 2636:1988 Sampling of venous and capillary blood for the determination of lead or cadmium concentration
- BS PD CEN/TS 16835-3:2015 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for venous whole blood-Isolated circulating cell free DNA from plasma
- 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
- 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
- SN-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
- BS PD 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
- DIN 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 version CEN/TS 17742:2022
- DANSK DS/ISO 23118:2021 Molecular in vitro diagnostic examinations – Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
- 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
- DANSK DS/EN ISO 25539-3:2012 Cardiovascular implants - Endovascular devices - Part 3: Vena cava filters
- DANSK DS/EN 14820:2004 Single-use containers for venous blood specimen collection
- 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
- CSA ISO 20186-3:2022 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 3: Isolated circulating cell free DNA from plasma
- DANSK DS/ISO 20186-3:2019 Molecular in vitro diagnostic examinations – Specifications for pre-examination processes for venous whole blood – Part 3: Isolated circulating cell free DNA from plasma
- SN-CEN/TS 16835-3:2015 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 3: Isolated circulating cell free DNA from plasma
- NS-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)
- DANSK DS/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)
- DANSK DS/CEN/TS 16835-3:2015 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasma
- NS-EN 14820:2004 Single-use containers for human venous blood specimen collection
- CAN/CSA-ISO 20186-3-2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasma
- AENOR UNE-EN 14820:2005 Single-use containers for human venous blood specimen collection
- AS 2411:1980 Determination of lead in venous blood (flame atomic absorption spectrometric method)
- 10/30196945 DC BS ISO 25539-3. Cardiovascular implants. Endovascular devices. Part 3. Vena cava filters
衛(wèi)生健康委員會, venous whole blood venous plasma
Xinjiang Provincial Standard of the People's Republic of China, venous whole blood venous plasma
GSO, venous whole blood venous plasma
- OS GSO 798:1997 CONTAINERS FOR PHARMACEUTICAL SOLUTIONS FOR INTRAVENOUS TRANSFUSION
- BH GSO ISO 23118:2023 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
- 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 797:1997 METHODS OF TESTING CONTAINERS FOR PHARMACEUTICAL SOLUTIONS FOR INTRAVENOUS TRANSFUSION
- GSO ISO 6710:2013 Single-use containers for venous blood specimen collection
- OS GSO ISO 6710:2013 Single-use containers for venous blood specimen collection
- GSO ISO 25539-3:2024 Cardiovascular implants — Endovascular devices — Part 3: Vena cava filters
- GSO ASTM F2172:2021 Standard Specification for Blood/Intravenous Fluid/Irrigation Fluid Warmers
- BH GSO ASTM F2172:2022 Standard Specification for Blood/Intravenous Fluid/Irrigation Fluid Warmers
Shanghai Provincial Standard of the People's Republic of China, venous whole blood venous plasma
Indonesia Standards, venous whole blood venous plasma
Korean Agency for Technology and Standards (KATS), venous whole blood venous plasma
- KS P ISO 6710:2009 Single-use containers for venous blood specimen collection
- KS P ISO 15674:2009 Cardiovascular implants and artificial organs-Hard-shell cardiotomy/venous reservoir systems(with/without filter) and soft venous reservoir bags
- KS P ISO 6710:2019 Single-use containers for human venous blood specimen collection
- KS P ISO 20186-3-2023 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 3: Isolated circulating cell free DNA from plasma
Jiangsu Provincial Standard of the People's Republic of China, venous whole blood venous plasma
British Standards Institution (BSI), venous whole blood venous plasma
- BS EN ISO 25539-3:2011 Cardiovascular implants. Endovascular devices. Vena cava filters
- BS EN ISO 25539-3:2012 Cardiovascular implants. Endovascular devices. Vena cava filters
- 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 EN ISO 23118:2021 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
- BS EN 14820:2004 Single-use containers for human venous blood specimen collection
- BS EN ISO 6710:2017 Single-use containers for human venous blood specimen collection
- PD 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
- BS EN 14280:2004 Single - use containers forhumanvenousblood specimen collection
- BS EN ISO 10555-3:1997 Sterile, single-use intravascular catheters. Central venous catheters
- 20/30375467 DC BS EN ISO 23118. Molecular in vitro diagnostic examinations. Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
- BS ISO 15674:2009 Cardiovascular implants and artificial organs - Hard-shell cardiotomy/venous reservoir systems (with/without filter) and soft venous reservoir bags
- BS ISO 15674:2016 Cardiovascular implants and artificial organs. Hard-shell cardiotomy/venous reservoir systems (with/without filter) and soft venous reservoir bags
Association Francaise de Normalisation, venous whole blood venous plasma
- NF S93-240:2005 Single-use containers for venous blood specimen collection.
- NF EN ISO 6710:2017 Single-use containers for human venous blood samples
- NF S93-240*NF EN ISO 6710:2017 Single-use containers for human venous blood specimen collection
- 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 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 EN ISO 25539-3:2012 Implants cardiovasculaires - Dispositifs endovasculaires - Partie 3 : filtres caves
- NF S94-203-3*NF EN ISO 25539-3:2012 Cardiovascular implants - Endovascular devices - Part 3 : vena cava filters
- NF S92-075-3*NF EN ISO 20186-3:2019 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3 : isolated circulating cell free DNA from plasma
- NF EN ISO 20186-3:2019 In vitro molecular diagnostic assays - Specifications for preanalytical processes for venous whole blood - Part 3: Circulating free DNA extracted from plasma
Professional Standard - Medicine, venous whole blood venous plasma
- YY 0603-2007 Cardiovascular implants and artificial organs-Hard-shell cardiotomy/venous reservoir systems(with/without filter)and soft venous reservoir bags
- YY 0603-2024 Cardiopulmonary bypass systems — Hard-shell cardiotomy/ venous reservoir systems (with/without filter) and soft venous reservoir bag
- YY 0603-2015 Cardiovascular implants and artificial organs.Hard-shell cardiotomy/ venous reservoir systems (with/without filter) and soft venous reservoir bags
- YY 0314-1999 Single-use containers for venous blood specimen collection
- YY/T 1856-2023 General safety requirements for blood, intravenous solution, and lavage fluid warmers
- YY 0314-2007 Single-use containers for human venous blood specimen collection
- YY/T0663.3-2016/ISO 25539-3:2011 Cardiovascular Implants Intravascular Devices Part 3: Vena Cava Filters
- YY/T 0314-2007(A1) Single-use containers for human venous blood specimen collection
- YY/T 0314-2007 Single-use containers for human venous blood specimen collection
Standard Association of Australia （SAA）, venous whole blood venous plasma
- AS 2636:1994 Sampling of venous and capillary blood for the determination of lead or cadmium concentration
- AS 2411:1993 Venous blood - Determination of lead content - Flame atomic absorption spectrometric method
VN-TCVN, venous whole blood venous plasma
- TCVN 7612-2007 Single-use containers for venous blood specimen collection
International Organization for Standardization (ISO), venous whole blood venous plasma
- ISO 15674:2016 Cardiovascular implants and artificial organs - Hard-shell cardiotomy/venous reservoir systems (with/without filter) and soft venous reservoir bags
- ISO 6710:1995 Single-use containers for venous blood specimen collection
- ISO 15674:2001 Cardiovascular implants and artificial organs - Hard-shell cardiotomy/venous reservoir systems (with/without filter) and soft venous reservoir bags
- ISO 15674:2016/Amd 1:2020 Cardiovascular implants and artificial organs — Hard-shell cardiotomy/venous reservoir systems (with/without filter) and soft venous reservoir bags — Amendment 1: Connectors
- ISO 15674:2009 Cardiovascular implants and artificial organs - Hard-shell cardiotomy/venous reservoir systems (with/without filter) and soft venous reservoir bags
- ISO 6710:2017 Single-use containers for human venous blood specimen collection
- ISO/CD 25539-3 Cardiovascular implants — Endovascular devices — Part 3: Vena cava filters
- ISO 23118:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
- ISO 25539-3:2011 Cardiovascular implants - Endovascular devices - Part 3: Vena cava filters
- ISO/DIS 25539-3:2023 Cardiovascular implants — Endovascular devices — Part 3: Vena cava filters
- ISO 10555-2:1996 Sterile, single-use intravascular catheters - Part 2: Angiographic catheters
European Committee for Standardization (CEN), venous whole blood venous plasma
- EN ISO 6710:2017 Single-use containers for human venous blood specimen collection
- 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
- prEN ISO 18703 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma
- PD CEN/TS 16945:2016 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for metabolomics in urine@ venous blood serum and plasma
- 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)
- EN 14820:2004 Single-use containers for human venous blood specimen collection
- EN ISO 25539-3:2011 Cardiovascular implants - Endovascular devices - Part 3: Vena cava filters (ISO 25539-3:2011)
US-AAMI, venous whole blood venous plasma
- ANSI/AAMI/ISO 15674:2009 Cardiovascular implants and artificial organs - Hard-shell cardiotomy/venous reservoir systems (with/without filter) and soft venous reservoir bags
ES-UNE, venous whole blood venous plasma
- 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 Espa?ola de Normalización in May of 2022.)
- 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)
- UNE-EN ISO 20186-3:2020 Molecular in-vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasma (ISO 20186-3:2019)
- UNE-EN ISO 6710:2018 Single-use containers for human venous blood specimen collection (ISO 6710:2017)
Japanese Industrial Standards Committee (JISC), venous whole blood venous plasma
- JIS T 3233:2005 Evacuated single-use containers for venous blood specimen collection
國家食品藥品監(jiān)督管理局, venous whole blood venous plasma
- YY/T 1618-2018 Disposable human venous blood sample collection needle
- YY/T 0663.3-2016 Cardiovascular Implants Intravascular Devices Part 3: Vena Cava Filters
Lithuanian Standards Office , venous whole blood venous plasma
- LST EN 14820-2004 Single-use containers for human venous blood specimen collection
- LST 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)
- LST EN ISO 25539-3:2012 Cardiovascular implants - Endovascular devices - Part 3: Vena cava filters (ISO 25539-3:2011)
AENOR, venous whole blood venous plasma
Danish Standards Foundation, venous whole blood venous plasma
- DS/EN ISO 25539-3:2012 Cardiovascular implants - Endovascular devices - Part 3: Vena cava filters
- DS/ISO 23118:2021 Molecular in vitro diagnostic examinations – Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
American National Standards Institute （ANSI), venous whole blood venous plasma
IT-UNI, venous whole blood venous plasma
- UNI EN ISO 23118:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
國家藥監(jiān)局, venous whole blood venous plasma
- YY/T 0314-2021 Disposable human venous blood sample collection container
General Administration of Quality Supervision, Inspection and Quarantine of the People‘s Republic of China, venous whole blood venous plasma
- GB/T 43279.3-2023 Specification for pre-examination procedures on venous whole blood for molecular in vitro diagnostic testing Part 3: Isolation of plasma circulating cell-free DNA
GOST, venous whole blood venous plasma
- GOST R 59778-2021 Procedures for taking samples of venous and capillary blood for laboratory tests
- GOST R ISO 23118-2023 Molecular in vitro diagnostic examinations. Requirements for the processes of the preanalytical stage of the study of the metabolomics of urine, serum and plasma of venous blood
KR-KS, venous whole blood venous plasma
AT-ON, venous whole blood venous plasma
- OENORM 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)
CH-SNV, venous whole blood venous plasma
- SN 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)
ZA-SANS, venous whole blood venous plasma
- SANS 1775-4:2009 Intravenous infusion and transfusion equipment (sterile-packed for single use) Part 4: Central venous pressure (CVP) monitoring sets
American Society for Testing and Materials (ASTM), venous whole blood venous plasma
- ASTM F2172-02 Standard Specification for Blood/Intravenous Fluid/Irrigation Fluid Warmers