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Database: 365,228(8 Aug 2026)

What does blood flow check

What does blood flow check, Total:53 items.

The international standard classification for "What does blood flow check" includes: Laboratory medicine , Medical Sciences and health care facilities in general .

The Chinese standard classification for "What does blood flow check" includes: Medical laboratory equipment , Medical sanitary products , Sanitation in general , Mechanics Measurement .


Group Standards of the People's Republic of China

  • T/CVMA 111.3-2023 Technical specification for physical examination of canine and feline—Part 3: Assessment of perfusion status
  • T/CAME 38-2021 Performance validation of nucleic acid testing in blood screening

Professional Standard - Agriculture

  • 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
  • 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
  • 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
  • 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
  • 4 OIE陆生动物诊断试验和疫苗手册-2005 r-interferon test for bovine tuberculosis hematological examination

Jiangsu Provincial Standard of the People's Republic of China

  • DB32/T 4331-2022 Technical specification for clinical quantitative coronary flow fraction (QFR) examination
  • DB32/T 4622.2-2023 Risk Management in the Blood Collection and Supply Process Part 2 Blood Donor Health Examination and Blood Collection Risk Control Specifications

其他未分类

  • BJY 201805 Supplementary test method for inspection items of cowhide-derived ingredients in Ejiao Buxue Oral Liquid

Jilin Provincial Standard of the People's Republic of China

  • DB22/T 3262-2021 Technical regulations for transvaginal ultrasound detection of postmenopausal vaginal bleeding

Professional Standard - Commodity Inspection

  • SN/T 0323.3-2007 Rules for the inspection of medical equipment for import and export - Part 3 : Plastics collapsible containers for human blood-Blood components conventional containers

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 360-2024 Guideline for enumeration of peripheral blood lymphocyte subsets by flow cytometry
  • WS/T 360-2011 Guidelines for peripheral lymphocyte subsets by flow cytometry

National Metrological Verification Regulations of the People's Republic of China

  • JJG 667-1997 Verification Regulation of Liquid Positive Displacement Flow Meter
  • JJG 667-2010 Liquid Positive Displacement Flowmeter

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 11327/2-1983 RUBBER STOPPERS FOR BLOOD, PLASMA AND SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS Apparence, smell and taste checking out
  • STAS 11326/4-1984 RUBBER STOPPERS FOR RECIPIENTS OF BLOOD, PLASMA AND AQUEOUS SOLUTIONS FOR INJECTIONS AND PERFUSIONS Hcmolityc impurities checking up
  • STAS 11326/7-1989 RUBBER STOPPERS FOR PARENTHERAL USE BLOOD AND PREPARATOION BOTTLES Microbiological proofing checking up

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

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 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 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

GSO

  • 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

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

US-CFR-file

  • CFR 33-150.100-2013 Navigation and navigable waters. Part150:Deepwater ports: operations. Section150.100:What are the requirements for inspecting deepwater ports?

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)

SCC

  • 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/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 16945:2016 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for metabolomics in urine, venous blood serum and plasma
  • BS PD CEN/TS 16835-1:2015 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for venous whole blood-Isolated cellular RNA
  • BS PD CEN/TS 16835-2:2015 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for venous whole blood-Isolated genomic DNA
  • 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
  • DIN EN ISO 23118 E:2020 Draft Document - 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

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

European Committee for Standardization (CEN)

  • 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 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 (ISO 20186-3:2019)

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
  • 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

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)

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)

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)

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
  • 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