venous whole blood venous plasma

venous whole blood venous plasma, Total:149 items.

The international standard classification for "venous whole blood venous plasma" includes: Medical Sciences and health care facilities in general , Implants for surgery, prosthetics and orthotics , Transfusion, infusion and injection equipment , Medical materials .

The Chinese standard classification for "venous whole blood venous plasma" includes: Sanitation in general , Extracorporeal circulation, artificial organ and prosthesis device , General and microsurgical devices , Medical apparatus and devices in general .

Group Standards of the People's Republic of China

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/CADERM 9001-2022 Arterial/venous rapid hemostatic dressing
T/CVMA 141-2024 Bovine jugular vein blood collection and infusion operating specifications

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
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)
DIN 58905-1 E:2015-12 Haemostaseology - Blood collection - Part 1: Preparation of plasma from citrated venous blood for coagulation testing

卫生健康委员会

WS/T 661-2020 Guidelines of venous blood specimen collection

Xinjiang Provincial Standard of the People's Republic of China

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

Shanghai Provincial Standard of the People's Republic of China

DB31/ 144-1994 Expanded polytetrafluoroethylene venous vessel

Jiangsu Provincial Standard of the People's Republic of China

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

Professional Standard - Medicine

YY/T0663.3-2016/ISO 25539-3:2011 Cardiovascular Implants Intravascular Devices Part 3: Vena Cava Filters
YY 0603-2015 Cardiovascular implants and artificial organs—Hard-shell cardiotomy/venous reservoir systems(with/without filter)and soft venous reservoir bags
YY/T 0314-2007(A1) Single-use containers for human venous blood specimen collection
YY 0603-2007 Cardiovascular implants and artificial organs - Hard-shell cardiotomy/venous reservoir systems (with/without filter) and soft venous reservoir bags
YY/T 0314-2007 Single-use containers for human venous blood specimen collection
YY 0314-2007 Single-use containers for human venous blood specimen collection
YY 0314-1999 Single-use containers for venous blood specimen collection
YY 0603-2024 Cardiopulmonary bypass systems — Hard-shell cardiotomy/ venous reservoir systems (with/without filter) and soft venous reservoir bag
YY/T 1856-2023 General requirements for the safety of blood/intravenous fluid/irrigationfluid warmers

国家食品药品监督管理局

YY/T 0663.3-2016 Cardiovascular implants-Endovascular devices-Part 3:Vena cava filters
YY/T 1618-2018 Single-use needles for human venous blood specimen collection

国家药监局

YY/T 0314-2021 Single-use containers for human venous blood specimen collection

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

GB/T 43279.3-2023 Molecular in vitro diagnostic examinations—Specifications for pre-examination processes for venous whole blood—Part 3: Isolated circulating cell free DNA from plasma

Military Standards (MIL-STD)

DOD A-A-53927-1989 INFUSOR, PRESSURE, BLOOD-INTRAVENOUS BAG
DOD A-A-54207-1990 CATHETER, CARDIOVASCULAR (VENOUS THROMBECTOMY)

German Institute for Standardization

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

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

GSO

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

Indonesia Standards

SNI ISO 6710:2010 Single-use containers for venous blood specimen collection

Korean Agency for Technology and Standards (KATS)

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

British Standards Institution (BSI)

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

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

Standard Association of Australia （SAA）

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

TCVN 7612-2007 Single-use containers for venous blood specimen collection

International Organization for Standardization (ISO)

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)

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

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

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 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)

JIS T 3233:2005 Evacuated single-use containers for venous blood specimen collection

Lithuanian Standards Office

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

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)

Danish Standards Foundation

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)

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

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

GOST

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

KS P ISO 6710-2019 Single-use containers for human venous blood specimen collection

AT-ON

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

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

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)

ASTM F2172-02 Standard Specification for Blood/Intravenous Fluid/Irrigation Fluid Warmers

Others: Venous Whole Blood and Venous Plasma,venous whole blood,venous whole blood,venous whole blood venous plasma