Plasma flow detection

Plasma flow detection, Total:81 items.

The international standard classification for "Plasma flow detection" includes: Transfusion, infusion and injection equipment , Radiographic equipment , Medical Sciences and health care facilities in general , Laboratory medicine , Implants for surgery, prosthetics and orthotics .

The Chinese standard classification for "Plasma flow detection" includes: General and microsurgical devices , Medical electronic equipment , Sanitation in general , Medical laboratory equipment , Health quarantine , Extracorporeal circulation, artificial organ and prosthesis device , Medical apparatus and devices in general .

Group Standards of the People's Republic of China

T/SHSYCXH 8-2022 Test method of human Natural Killer cells and Natural Killer T cells from peripheral blood-Flow cytometry
T/CSBME 057-2022 Adsorption resin for hemoperfusion or plasma perfusion devices
T/SHSYCXH 7-2022 Test method of human monocyte populations from peripheral blood-Flow cytometry

Jilin Provincial Standard of the People's Republic of China

DB22/T 3262-2021 Technical regulations for transvaginal ultrasound detection of postmenopausal vaginal bleeding
DB22/T 2915-2018 Technical requirements for blood testing of blood donor dogs
DB22/T 2566-2016 Multiple PCR method for detection of Haemophilus influenzae type b nucleic acid

Professional Standard - Medicine

YY/T 1143-2008 Bridge type impedance blood flow recorder
YY/T 1078-2008 Direct impedance blood flow recorder
YY 0326.1-2002 Plasmapheresis centrifuge appararus for single use - Part 1: Centrifuge bowl
YY 0326.3-2005 Plasmapheresis centrifuge apparatus for single use-
YY 91143-1999 Bridge type impedance blood flow recorder
YY 91078-1999 Direct impedance blood flow recorder
YY/T 0326-2017 Plasmapheresis centrifuge apparatus for single use
YY 0326.2-2002 Plasmapheresis centrifuge appararus for single use--Part 2:Plasma tubing

National Health Commission of the People's Republic of China

WST 360:2011 Guidelines for detection of peripheral blood lymphocyte subsets by flow cytometry

Professional Standard - Hygiene

WS/T 358-2011 Immunoassay of serum or plasma lipoprotein(a)
WS/T 360-2011 Guidelines for peripheral lymphocyte subsets by flow cytometry
WS/T 360-2024 Guideline for enumeration of peripheral blood lymphocyte subsets by flow cytometry

Professional Standard - Aquaculture

SC 1002-1992 Detection method of grass carp hemorrhagic disease tissue plasma inactivated vaccine

Professional Standard - Agriculture

227药典四部-2020 3300 Microbiological Inspection Method 3306 Technical Requirements for Human Plasma Virus Nucleic Acid Detection for Production of Blood Products
236药典四部-2015 3300 Microbiological Inspection Method 3306 Technical Requirements for Human Plasma Virus Nucleic Acid Detection for Production of Blood Products
278药典三部-2020 Microbiological Examination Method 3306 General Rules for the Technical Requirements for Human Plasma Virus Nucleic Acid Detection in the Production of Blood Products 103
255药典三部-2015 Microbiological Examination Method 3306 General Rules for the Technical Requirements for Human Plasma Virus Nucleic Acid Detection in the Production of Blood Products 103

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）

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

Jiangsu Provincial Standard of the People's Republic of China

DB32/T 3762.15-2021 Technical specifications for SARS-CoV-2 detection―Part 15:Serum/Plasma IgM and IgG antibodies test procedure by MCLIA

Liaoning Provincial Standard of the People's Republic of China

DB21/T 2534-2015 Fluorescent PCR detection method for deer epidemic hemorrhagic disease virus

National Metrological Technical Specifications of the People's Republic of China

JJF 1372-2012 Calibration Specification for Instrument of Testing Mortar-strength by Penetration Resistance Method

Professional Standard - Commodity Inspection

SN/T 2777-2011 Detection of Epidemic Hemorrhagic Fever Virus (EHFV) In Imported Rodents-Method of Nested RT-PCR

中华人民共和国国家卫生和计划生育委员会

WST 358:2011 Immunoassay of serum (plasma) lipoprotein(a).pdf

国家质量监督检验检疫总局

SN/T 4823-2017 Detection method for bovine factor Ⅺ deficiency by nested PCR

中华人民共和国国家质量监督检验检疫总局、中国国家标准化管理委员会

GB 12260-2017 Cardiopulmonary bypass systems—Roller blood pump

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

SCC

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
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/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
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/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 16835-3:2015 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for venous whole blood-Isolated circulating cell free DNA from plasma
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)
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
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
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 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
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

RO-ASRO

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 11326/2-1985 RUBBER STOPPERS FOR BLOOD, PLASMA AND AQUEOUS SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS Pyrogenic impurities checking up
STAS 11326/4-1984 RUBBER STOPPERS FOR RECIPIENTS OF BLOOD, PLASMA AND AQUEOUS SOLUTIONS FOR INJECTIONS AND PERFUSIONS Hcmolityc impurities checking up
STAS 11327/2-1983 RUBBER STOPPERS FOR BLOOD, PLASMA AND SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS Apparence, smell and taste checking out

British Standards Institution (BSI)

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 20186-3:2019 Molecular in-vitro diagnostic examinations. Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free DNA from plasma
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
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

German Institute for Standardization

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 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 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 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

GSO

GSO ISO 23118:2023 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
BH GSO ISO 23118:2023 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma

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

European Committee for Standardization (CEN)

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)
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

Association Francaise de Normalisation

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

ES-UNE

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-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.)

Danish Standards Foundation

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

Korean Agency for Technology and Standards (KATS)

KS F 2433-2018 Standard test method for bleeding and expansion ratios of grouting mortar

International Organization for Standardization (ISO)

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

Lithuanian Standards Office

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)

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)