venous whole blood

venous whole blood, Total:257 items.

In the international standard classification, venous whole blood involves: Laboratory medicine, Medical sciences and health care facilities in general, Materials for aerospace construction, Precision mechanics, Medical equipment, Veterinary medicine, Farming and forestry, Pharmaceutics, Construction materials, Metrology and measurement in general, Vocabularies, Horology.

British Standards Institution (BSI), venous whole blood

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
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 ISO 25539-3:2012 Cardiovascular implants. Endovascular devices. Vena cava filters
BS EN ISO 25539-3:2011 Cardiovascular implants. Endovascular devices. Vena cava filters
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
BS EN 14280:2004 Single - use containers forhumanvenousblood specimen collection
BS EN ISO 10555-3:1997 Sterile, single-use intravascular catheters. Central venous catheters
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 ISO 20186-1:2019 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for venous whole blood - Isolated cellular RNA
BS EN ISO 20186-2:2019 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for venous whole blood - Isolated genomic DNA
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 EN ISO 10555-3:2013 Intravascular catheters. Sterile and single-use catheters. Central venous catheters
BS ISO 15674:2016 Cardiovascular implants and artificial organs. Hard-shell cardiotomy/venous reservoir systems (with/without filter) and soft venous reservoir bags
BS ISO 15674:2009 Cardiovascular implants and artificial organs - Hard-shell cardiotomy/venous reservoir systems (with/without filter) and soft venous reservoir bags
PD CEN/TS 17390-2:2020 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood. Isolated DNA
BS ISO 15674:2016+A1:2020 Cardiovascular implants and artificial organs — Hard - shell cardiotomy / venous reservoir systems (with / without filter) and soft venous reservoir bags
BS ISO 18241:2016 Cardiovascular implants and extracorporeal systems. Cardiopulmonary bypass systems. Venous bubble traps
BS ISO 18241:2016+A1:2019 Cardiovascular implants and extracorporeal systems — Cardiopulmonary bypass systems — Venous bubble traps
PD CEN/TS 17390-1:2020 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood. Isolated RNA
BS ISO 15675:2016+A1:2020 Cardiovascular implants and artificial organs — Cardiopulmonary bypass systems — Arterial blood line filters

European Committee for Standardization (CEN), venous whole blood

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
prEN ISO 18703 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
EN ISO 25539-3:2011 Cardiovascular implants - Endovascular devices - Part 3: Vena cava filters (ISO 25539-3:2011)
EN ISO 6710:2017 Single-use containers for human venous blood specimen collection
EN 14820:2004 Single-use containers for human venous blood specimen collection
prEN ISO 25539-3 Cardiovascular implants - Endovascular devices - Part 3: Vena cava filters (ISO/DIS 25539-3:2023)
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)
prCEN ISO/TS 7552-2 Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood -- Part 2: Isolated DNA
prCEN ISO/TS 7552-1 Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood -- Part 1: Isolated RNA
EN 865:1997 Pulse Oximeters - Particular Requirements
PD CEN/TS 16835-3:2015 Molecular in vitro diagnostic e xaminations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasma
EN ISO 10555-3:2013 Intravascular catheters - Sterile and single-use catheters - Part 3: Central venous catheters
PD CEN/TS 16835-1:2015 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNA

ES-UNE, venous whole blood

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.)
UNE-EN ISO 6710:2018 Single-use containers for human venous blood specimen collection (ISO 6710:2017)
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 20186-1:2019 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNA (ISO 20186-1:2019)
UNE-EN ISO 20186-2:2020 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNA (ISO 20186-2:2019)

German Institute for Standardization, venous whole 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 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 58905-1:2000 Haemostaseology - Blood collection - Part 1: Preparation of plasma from citrated venous blood for coagulation testing
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 58914-1:2000-03 Haemostaseology - Determination of thrombin time - Part 1: Reference measurement procedure for the determination in plasma from citrated venous blood
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 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 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 Haemostaseology - Determination of thrombin time - Part 1: Reference measurement procedure for the determination in plasma from citrated venous blood
DIN EN ISO 25539-3:2023-08 Cardiovascular implants - Endovascular devices - Part 3: Vena cava filters (ISO/DIS 25539-3:2023); German and English version prEN ISO 25539-3:2023 / Note: Date of issue 2023-07-14*Intended as replacement for DIN EN ISO 25539-3 (2012-03).
DIN EN ISO 25539-3:2023 Cardiovascular implants - Endovascular devices - Part 3: Vena cava filters (ISO/DIS 25539-3:2023); German and English version prEN ISO 25539-3:2023
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 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 58910-2:2000 Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 2: Reference measurement procedure for the determination in 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 6710:2017-12 Single-use containers for human venous blood specimen collection (ISO 6710:2017); German version EN ISO 6710:2017
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)
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 25539-3:2012 Cardiovascular implants - Endovascular devices - Part 3: Vena cava filters (ISO 25539-3:2011); German version EN ISO 25539-3:2011
DIN EN ISO 20186-1:2019-08 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNA (ISO 20186-1:2019); German version EN ISO 20186-1:2019
DIN EN ISO 20186-2:2019-08 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNA (ISO 20186-2:2019); German version EN ISO 20186-2:2019
DIN EN ISO 10555-3:2013-11 Intravascular catheters - Sterile and single-use catheters - Part 3: Central venous catheters (ISO 10555-3:2013); German version EN ISO 10555-3:2013
DIN 58903:2000 Haemostaseology - Deficient plasma - Requirements, preparation
DIN 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); German version EN ISO 23118:2021
DIN EN ISO 6710:2017 Single-use containers for human venous blood specimen collection (ISO 6710:2017); German version EN ISO 6710:2017

Group Standards of the People's Republic of China, venous whole blood

T/CADERM 9001-2022 Arterial/venous rapid hemostatic dressing
T/CAMDI 104-2023 Rubber sleeve for venous blood sample collection needle
T/CVMA 142-2024 Bovine tail vein blood collection and injection operating instructions
T/CVMA 141-2024 Bovine jugular vein blood collection and infusion operating specifications
T/CRHA 028-2023 Risk assessment techniques for venous thromboembolism in adult inpatients
T/SBX 075-2023 Pulse Oximeter Calibration Specifications
T/CADERM 3034-2020 Specifications of prevention and treatment for deep vein thrombosis in patients with severe trauma
T/SHNA 0004-2023 Invasive arterial blood pressure monitoring methods
T/CVMA 79-2021 Technical specification for canine direct arterial blood pressure measurement
T/HBAS 018-2023 Technical specification for wrist pulse rate blood oxygen monitor
T/CHAS 10-2-24-2018 Quality and safety management of Chinese hospital——Part 2-24: Patient service—— Prevention and treatment of venous thromboembolism of inpatient

Standard Association of Australia （SAA）, venous whole blood

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
AS ISO 9919:2004 Pulse oximeters for medical use - Requirements

Military Standards (MIL-STD), venous whole blood

DOD A-A-54207-1990 CATHETER, CARDIOVASCULAR (VENOUS THROMBECTOMY)
DOD A-A-53927-1989 INFUSOR, PRESSURE, BLOOD-INTRAVENOUS BAG
DOD A-A-54964-1994 MONITORING SET, ARTERIAL BLOOD GAS SAMPLING AND PRESSURE

Xinjiang Provincial Standard of the People's Republic of China, venous whole blood

DB65/T 3793-2015 Technical specification for oxtail vein blood collection

卫生健康委员会, venous whole blood

WS/T 661-2020 Venous blood specimen collection guide
WS/T 623-2018 Use of whole blood and blood components

Professional Standard - Medicine, venous whole blood

YY 0603-2015 Cardiovascular implants and artificial organs.Hard-shell cardiotomy/ venous reservoir systems (with/without filter) and soft venous reservoir bags
YY 0603-2007 Cardiovascular implants and artificial organs-Hard-shell cardiotomy/venous reservoir systems(with/without filter)and soft venous reservoir bags
YY/T0663.3-2016/ISO 25539-3:2011 Cardiovascular Implants Intravascular Devices Part 3: Vena Cava Filters
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/T 0314-2007 Single-use containers for human venous blood specimen collection
YY/T 0314-2007(A1) Single-use containers for human venous blood specimen collection
YY 0314-2007 Single-use containers for human venous blood specimen collection
YY 0612-2007 Single-use receptacles for human arterial blood specimen collection
YY 0285.3-1999 Sterile,single-use intravasoular catheters.Part 3:Central venous catheters

Korean Agency for Technology and Standards (KATS), venous whole blood

KS P ISO 6710:2009 Single-use containers for venous blood specimen collection
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
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 9919-2007(2012) Pulse oximeters for medical use－Requirements
KS P ISO 10555-3:2007 Sterile, single-use intravascular catheters－Part 3：Central venous catheters
KS P ISO 15674:2020 Cardiovascular implants and artificial organs — Hard-shell cardiotomy/venous reservoir systems(with/without filter) and soft venous reservoir bags
KS P ISO 10555-3:2018 Intravascular catheters — Sterile and single-use catheters — Part 3: Central venous catheters
KS P ISO 18241:2018 Cardiovascular implants and extracorporeal systems — Cardiopulmonary bypass systems — Venous bubble traps
KS P ISO 10555-3-2023 Intravascular catheters — Sterile and single-use catheters — Part 3: Central venous catheters
KS P ISO 18241-2023 Cardiovascular implants and extracorporeal systems — Cardiopulmonary bypass systems — Venous bubble traps
KS P ISO 15675:2009 Cardiovascular implants and artificial organs-Cardiopulmonary bypass systems-Arterial blood line filters
KS P ISO 15675:2020 Cardiovascular implants and artificial organs — Cardiopulmonary bypass systems — Arterial blood line filters

Indonesia Standards, venous whole blood

SNI ISO 6710:2010 Single-use containers for venous blood specimen collection
SNI 16-6360-2000 Pulse oximeters for medical use

Jiangsu Provincial Standard of the People's Republic of China, venous whole blood

DB3201/T 297-2019 Technical regulations for poultry wing venous blood collection

Shanghai Provincial Standard of the People's Republic of China, venous whole blood

DB31/ 144-1994 Expanded polytetrafluoroethylene venous vessel
DB31/ 145-1994 expanded polytetrafluoroethylene arteries

未注明发布机构, venous whole blood

DIN 58905-1 E:2015-12 Haemostaseology - Blood collection - Part 1: Preparation of plasma from citrated venous blood for coagulation testing
ANSI/AAMI/ISO 25539-3:2011(2015) Cardiovascular implants — Endovascular devices — Part 3: Vena cava filters
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
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)
JIS T 3233:2023 Evacuated single-use containers for human venous blood specimen collection
DIN EN ISO 10555-3 Berichtigung:2003 Sterile single-use intravascular catheters – Part 3: Central venous catheters
DIN EN ISO 10555-3:1997 Sterile single-use intravascular catheters Part 3: Central venous catheters
ANSI/AAMI/ISO 15674:2016 Cardiovascular implants and artificial organs— Hard-shell cardiotomy/ venous reservoir systems (with/without filter) and soft venous reservoir bags
ANSI/AAMI/ISO 18241:2016 Cardiovascular implants and extracorporeal systems—Cardiopulmonary bypass systems—Venous bubble traps
DIN 58903 E:2019-04 Haemostaseology - Deficient plasma - Requirements, preparation
DIN EN ISO 20186-1 E:2017-02 Procedure Specification for Preliminary Examination of Venous Whole Blood for Molecular In Vitro Diagnostic Examination Part 1: Isolated Cellular RNA (Draft)
ANSI/AAMI/ISO 15675:2016 Cardiovascular implants and artificial organs— Cardiopulmonary bypass systems—Arterial blood line filters
DIN EN ISO 20186-2 E:2017-02 Procedure Specification for Preliminary Examination of Venous Whole Blood for Molecular In Vitro Diagnostic Examination Part 2: Isolated Genomic DNA (Draft)

VN-TCVN, venous whole blood

TCVN 7612-2007 Single-use containers for venous blood specimen collection
TCVN 7609-3-2007 Sterile, single-use intravascular catheters.Part 3: Central venous catheters

Association Francaise de Normalisation, venous whole blood

NF S93-240:2005 Single-use containers for venous blood specimen collection.
NF EN ISO 6710:2017 Récipients à usage unique pour prélèvements de sang veineux humain
NF S94-203-3*NF EN ISO 25539-3:2012 Cardiovascular implants - Endovascular devices - Part 3 : vena cava filters
NF EN ISO 25539-3:2012 Implants cardiovasculaires - Dispositifs endovasculaires - Partie 3 : filtres caves
NF S93-240*NF EN ISO 6710:2017 Single-use containers for human venous blood specimen collection
NF EN ISO 23118:2021 Analyses de diagnostic moléculaire in vitro - Spécifications relatives aux processus préanalytiques pour l'analyse du métabolome dans l'urine et le sang veineux (sérum et 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 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 Analyses de diagnostic moléculaire in vitro - Spécifications relatives aux processus préanalytiques pour le sang total veineux - Partie 3 : ADN libre circulant extrait du plasma
NF S94-203-1:2009 Cardiovascular implants - Endovascular devices - Part 1 : endovascular prostheses.
NF S92-075-1*NF EN ISO 20186-1:2019 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1 : isolated cellular RNA
XP S92-075-1*XP CEN/TS 16835-1:2015 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1 : isolated cellular RNA
NF EN ISO 20186-1:2019 Analyses de diagnostic moléculaire in vitro - Spécifications relatives aux processus préanalytiques pour le sang total veineux - Partie 1 : ARN cellulaire extrait
NF S93-031-3*NF EN ISO 10555-3:2013 Intravascular catheters - Sterile and single-use catheters - Part 3: central venous catheters
NF S93-031-3:1997 Sterile, single-use intravascular catheters. Part 3 : central venous catheters.
NF S92-075-2*NF EN ISO 20186-2:2019 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2 : isolated genomic DNA
XP S92-075-2*XP CEN/TS 16835-2:2015 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2 : isolated genomic DNA
NF EN ISO 20186-2:2019 Analyses de diagnostic moléculaire in vitro - Spécifications relatives aux processus préanalytiques pour le sang total veineux - Partie 2 : ADN génomique extrait

Danish Standards Foundation, venous whole blood

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
DS/EN ISO 10555-3:2013 Intravascular catheters - Sterile and single-use catheters - Part 3: Central venous catheters
DS/ISO 15674:2009 Cardiovascular implants and artificial organs - Hard-shell cardiotomy/venous reservoir systems (with/without filter) and soft venous reservoir bags
DS/ISO 15675:2009 Cardiovascular implants and artificial organs - Cardiopulmonary bypass systems - Arterial blood line filters

International Organization for Standardization (ISO), venous whole blood

ISO/CD 25539-3 Cardiovascular implants — Endovascular devices — Part 3: Vena cava filters
ISO 15674:2009 Cardiovascular implants and artificial organs - Hard-shell cardiotomy/venous reservoir systems (with/without filter) and soft venous reservoir bags
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 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 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
ISO 6710:2017 Single-use containers for human venous blood specimen collection
ISO 23118:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
ISO 9919:1992 Pulse oximeters for medical use; requirements
ISO 20186-1:2019 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 1: Isolated cellular RNA
ISO 10555-3:1996 Sterile, single-use intravascular catheters - Part 3: Central venous catheters
ISO 20186-2:2019 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 2: Isolated genomic DNA
ISO 18241:2016 Cardiovascular implants and extracorporeal systems - Cardiopulmonary bypass systems - Venous bubble traps
ISO 10555-3:2013 Intravascular catheters - Sterile and single-use catheters - Part 3: Central venous catheters

American National Standards Institute （ANSI), venous whole blood

ANSI/AAMI/ISO 25539-3:2012 Cardiovascular implants - Endovascular devices - Part 3: Vena Cava Filters

国家食品药品监督管理局, venous whole blood

YY/T 0663.3-2016 Cardiovascular Implants Intravascular Devices Part 3: Vena Cava Filters
YY/T 1618-2018 Disposable human venous blood sample collection needle
YY 0285.3-2017 Intravascular Catheters Single Use Sterile Catheters Part 3: Central Venous Catheters

US-AAMI, venous whole blood

ANSI/AAMI/ISO 15674:2009 Cardiovascular implants and artificial organs - Hard-shell cardiotomy/venous reservoir systems (with/without filter) and soft venous reservoir bags

GOST, venous whole blood

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

Lithuanian Standards Office , venous whole blood

LST EN 14820-2004 Single-use containers for human venous blood specimen collection
LST EN ISO 25539-3:2012 Cardiovascular implants - Endovascular devices - Part 3: Vena cava filters (ISO 25539-3:2011)
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 10555-3:2001 Sterile, single-use intravascular catheters - Part 3: Central venous catheters (ISO 10555-3:1996)

Japanese Industrial Standards Committee (JISC), venous whole blood

JIS T 3233:2005 Evacuated single-use containers for venous blood specimen collection
JIS T 3232:2011 Blood filters for cardiopulmonary bypass systems
JIS T 3232:2016 Blood filters for cardiopulmonary bypass systems

AENOR, venous whole blood

UNE-EN 14820:2005 Single-use containers for human venous blood specimen collection
UNE-EN ISO 25539-3:2012 Cardiovascular implants - Endovascular devices - Part 3: Vena cava filters (ISO 25539-3:2011)

国家药监局, venous whole blood

YY/T 0314-2021 Disposable human venous blood sample collection container
YY/T 0612-2022 Disposable human arterial blood sample collector (arterial blood gas needle)
YY/T 1747-2021 Neurovascular ImplantsIntracranial Artery Stents
YY/T 1758-2020 Cardiovascular Implants Pulmonary Artery Valved Conduits

GSO, venous whole blood

GSO ISO 6710:2013 Single-use containers for venous blood specimen collection
GSO ASTM F2172:2021 Standard Specification for Blood/Intravenous Fluid/Irrigation Fluid Warmers
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 10555-3:2013 Intravascular catheters -- Sterile and single-use catheters -- Part 3: Central venous catheters
GSO ISO 18241:2021 Cardiovascular implants and extracorporeal systems — Cardiopulmonary bypass systems — Venous bubble traps
GSO ISO 15675:2015 Cardiovascular implants and artificial organs -- Cardiopulmonary bypass systems -- Arterial blood line filters

KR-KS, venous whole blood

KS P ISO 6710-2019 Single-use containers for human venous blood specimen collection
KS P ISO 15674-2020 Cardiovascular implants and artificial organs — Hard-shell cardiotomy/venous reservoir systems(with/without filter) and soft venous reservoir bags
KS P ISO 20186-1-2022 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 1: Isolated cellular RNA
KS P ISO 10555-3-2018 Intravascular catheters — Sterile and single-use catheters — Part 3: Central venous catheters
KS P ISO 18241-2018 Cardiovascular implants and extracorporeal systems — Cardiopulmonary bypass systems — Venous bubble traps
KS P ISO 10555-3-2018(2023) Intravascular catheters — Sterile and single-use catheters — Part 3: Central venous catheters
KS P ISO 15675-2020 Cardiovascular implants and artificial organs — Cardiopulmonary bypass systems — Arterial blood line filters

General Administration of Quality Supervision, Inspection and Quarantine of the People‘s Republic of China, venous whole blood

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
GBZ 291-2017 Diagnosis of occupational femoral venous thrombosis, femoral occlusive disease, or lymphatic occlusive disease
GB 18469-2001 Standards for whole blood and blood components quality
GB 18469-2012 Quality requirements for whole blood and blood components
GB/T 43279.1-2023 Specification for pre-test procedures on venous whole blood for molecular in vitro diagnostic testing Part 1: Isolation of cellular RNA
GB/T 43279.2-2023 Specification for pre-test procedures on venous whole blood for molecular in vitro diagnostic testing Part 2: Isolation of genomic DNA

IT-UNI, venous whole blood

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

American Society for Testing and Materials (ASTM), venous whole blood

ASTM F2172-02 Standard Specification for Blood/Intravenous Fluid/Irrigation Fluid Warmers
ASTM F2172-02(2011) Standard Specification for Blood/Intravenous Fluid/Irrigation Fluid Warmers
ASTM F1415-92 Standard Specification for Pulse Oximeters

SCC, venous whole blood

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
CSA ISO 20186-1:2022 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 1: Isolated cellular RNA
CSA ISO 20186-2:2022 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 2: Isolated genomic DNA

Professional Standard - Agriculture, venous whole blood

718药典中药成方制剂卷-2010 Sections on Internal Medicine 15. Blood Regulating Agents (3) Yiqi Huoxue Xueshuan Xinmaining Capsules
1093药典中药成方制剂卷-2010 Monographs on Surgery VI. Huoxue Tongmai Tongsaimai Tablets
1092药典中药成方制剂卷-2010 Discussion on Surgery VI. Huoxue Tongmai Tongmai Bao Ointment
659药典中药成方制剂卷-2010 Sections on Internal Medicine 15. Blood Regulating Agents (1) Huoxue Huayu Tongmai Granules
691药典中药成方制剂卷-2010 Sections on Internal Medicine XV. Blood Regulating Agents (2) Promoting Qi and Activating Blood Guanmaining Tablets
676药典中药成方制剂卷-2010 Sections on Internal Medicine XV. Blood Regulating Agents (1) Activating Blood and Huayu Xinmaitong Tablets
701药典中药成方制剂卷-2010 Sections on Internal Medicine XV. Blood Regulating Agents (2) Xingqi Huoxue Lemai Granules
737药典中药成方制剂卷-2010 Sections on Internal Medicine 15. Blood Regulating Agents (3) Yiqi Huoxue Mailuotong Granules
675药典中药成方制剂卷-2010 Sections on Internal Medicine XV. Blood Regulating Agents (1) Activating Blood and Removing Blood Stasis Zhuyu Tongmai Capsules
741药典中药成方制剂卷-2010 Sections on Internal Medicine 15. Blood Regulating Agents (3) Yiqi Huoxue Ruanmailing Oral Liquid
1091药典中药成方制剂卷-2010 Monographs on Surgery VI. Huoxue Tongmailuoning Injection
1095药典中药成方制剂卷-2010 Monographs on Surgery VI. Huoxuetongmailuoshutong Granules
1090药典中药成方制剂卷-2010 Chapter 6: Huoxue Tongmailuoning Oral Liquid
728药典中药成方制剂卷-2010 Sections on Internal Medicine XV. Blood Regulating Agents (3) Guanxinjing Tablets for Yiqi Huoxue
780药典中药成方制剂卷-2010 Sections on Internal Medicine XV. Blood Regulating Agents (VI) Promoting Blood and Resolving Phlegm, Expelling Wind and Naomaitai Capsules
753药典中药成方制剂卷-2010 Sections on Internal Medicine 15. Blood Regulating Agents (4) Yiqi, Yangyin, Activating Blood and Shengmai Injection
1302药典化学药和生物制品卷-2010 Chapter 18 Biological Products 3. Blood Products Human Immunoglobulin for Intravenous Injection
746药典中药成方制剂卷-2010 Sections on Internal Medicine XV. Blood Regulating Agents (3) Yiqi Huoxue Yiqi Fumai Capsules (Granules)
760药典中药成方制剂卷-2010 Sections on Internal Medicine 15. Blood Regulating Agents (4) Yixin Tongmai Granules
757药典中药成方制剂卷-2010 Sections on Internal Medicine 15. Blood Regulating Agents (4) Yixin Fumai Granules for Yiqi, Yangyin, Huoxue
765药典中药成方制剂卷-2010 Sections on Internal Medicine 15. Blood Regulating Agents (4) Guanxin Shengmai Oral Liquid

未注明发布机构, venous whole blood

DIN 58905-1 E:2015-12 Haemostaseology - Blood collection - Part 1: Preparation of plasma from citrated venous blood for coagulation testing
ANSI/AAMI/ISO 25539-3:2011(2015) Cardiovascular implants — Endovascular devices — Part 3: Vena cava filters
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
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)
JIS T 3233:2023 Evacuated single-use containers for human venous blood specimen collection
DIN EN ISO 10555-3 Berichtigung:2003 Sterile single-use intravascular catheters – Part 3: Central venous catheters
DIN EN ISO 10555-3:1997 Sterile single-use intravascular catheters Part 3: Central venous catheters
ANSI/AAMI/ISO 15674:2016 Cardiovascular implants and artificial organs— Hard-shell cardiotomy/ venous reservoir systems (with/without filter) and soft venous reservoir bags
ANSI/AAMI/ISO 18241:2016 Cardiovascular implants and extracorporeal systems—Cardiopulmonary bypass systems—Venous bubble traps
DIN 58903 E:2019-04 Haemostaseology - Deficient plasma - Requirements, preparation
DIN EN ISO 20186-1 E:2017-02 Procedure Specification for Preliminary Examination of Venous Whole Blood for Molecular In Vitro Diagnostic Examination Part 1: Isolated Cellular RNA (Draft)
ANSI/AAMI/ISO 15675:2016 Cardiovascular implants and artificial organs— Cardiopulmonary bypass systems—Arterial blood line filters
DIN EN ISO 20186-2 E:2017-02 Procedure Specification for Preliminary Examination of Venous Whole Blood for Molecular In Vitro Diagnostic Examination Part 2: Isolated Genomic DNA (Draft)

AT-ON, venous whole blood

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

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)

US-CLSI, venous whole blood

CLSI H59-P-2010 Quantitative D-dimer for the Exclusion of Venous Thromboembolic Disease

Hebei Provincial Standard of the People's Republic of China, venous whole blood

DB13/T 5203-2020 Intramuscular injection and anterior vena cava blood collection technology operating procedures in pig neck

ZA-SANS, venous whole blood

SANS 1775-4:2009 Intravenous infusion and transfusion equipment (sterile-packed for single use) Part 4: Central venous pressure (CVP) monitoring sets

RU-GOST R, venous whole blood

GOST ISO 10555-3-2021 Intravascular sterile and single-use catheters. Part 3. Central venous catheters
GOST R ISO 10555.3-1999 Sterile, single-use intravascular catheters. Part 3. Central venous catheters
GOST ISO 6710-2011 Single-use containers for venous blood specimen collection. Technical requirements and test methods
GOST 31515.3-2012 Non-invasive sphygmomanometers (measuring devices of arterial pressure). Part 3. Supplementary requirements for electro-mechanical blood pressure measuring systems
GOST 31515.1-2012 Non-invasive sphygmomanometers (measuring devices of arterial pressure). Part 1. General requirements

中华人民共和国国家卫生和计划生育委员会, venous whole blood

WS/T 122-1999 Quantitative determination of hemoglobin in whole blood

CEN - European Committee for Standardization, venous whole blood

EN ISO 20186-1:2019 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNA
EN ISO 20186-2:2019 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNA

TH-TISI, venous whole blood

TIS 1703.3-1998 Sterile, single.use intravascular catheters.part 3: central venous catheters

Jilin Provincial Standard of the People's Republic of China, venous whole blood

DB22/T 3223-2021 Arterial blood sample collection nursing norms

GOSTR, venous whole blood

GOST ISO 10555-3-2011 Sterile, single-use intravascular catheters. Part 3. Central venous catheters

国家卫生计生委, venous whole blood

WS/T 550-2017 Guidelines for quality monitoring of whole blood and blood components

PK-PSQCA, venous whole blood

PS 456-1964 STRAIGHT ARTERY (HAEMOSTATIC) FORCEPS SPENCER WELLS PATTERN (SCREW JOINT)