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Definition of Cell Generation

Definition of Cell Generation, Total:134 items.

The international standard classification for "Definition of Cell Generation" includes: Biology. Botany. Zoology , Textile fabrics , Transfusion, infusion and injection equipment , Laboratory medicine , Medical Sciences and health care facilities in general .

The Chinese standard classification for "Definition of Cell Generation" includes: Biological agent and blood products , Basic standards and general methods , Basic Subject in general , General and microsurgical devices , Medical laboratory equipment , Sanitation in general .


国家市场监督管理总局、中国国家标准化管理委员会

  • GB/T 39103-2020 Superfine woven wool fabric labelling—Requirements for Super S code definition
  • GB/T 39729-2020 General requirements for measurement of cell purity—Flow cytometry
  • GB/T 38484-2020 Determination of the biological activity for plant hormone-related secondary metabolites. Cytological method
  • GB/T 39730-2020 General requirements for cell counting—Flow cytometry

Group Standards of the People's Republic of China

  • T/SDHCST 006-2023 Procedures for Single Dose Toxicity Testing of the Cell Therapy Medical Products
  • T/SHSYCXH 8-2022 Test method of human Natural Killer cells and Natural Killer T cells from peripheral blood-Flow cytometry
  • T/CECCEDA 002-2023 Manufacture practice of single-use materials in CAR-T production
  • T/LNSI 004-2023 Human cytokine induced killer cell
  • T/CECCEDA 003.1-2023 Technical requirement of single-use materials in CAR-T production Part 1: Cell frozen bag、Cell storage bag
  • T/CSCB 0008-2021 Primary human hepatocyte
  • T/ZZB 1653-2020 Disposable cell cryogenic vials(Polypropylene)
  • T/CRHA 001-2021 Human mesenchymal stem cell derived small extracellular vesicles
  • T/CIET 503-2024 Specification for preparation and quality identification of hepatic progenitor cells derived from human induced pluripotent stem cells
  • T/CEAC 039-2024 Stem cell identification methods
  • T/LNSI 004-2024 Human cytokine induced killer cell
  • T/WEBIO 0001-2023 Specification of human primary cell preparation and quality control
  • T/CRHA 002-2021 Human pluripotent stem cell derived small extracellular vesicles
  • T/SHSYCXH 7-2022 Test method of human monocyte populations from peripheral blood-Flow cytometry
  • T/CECCEDA 003.2-2023 Technical requirement of single-use materials in CAR-T production Part 2: Cell sap culture tank
  • T/CIET 502-2024 Preparation and quality identification of mesenchymal stem cells derived from human induced pluripotent stem cells

Professional Standard - Medicine

Professional Standard - Agriculture

  • 163兽药典 三部-2015 Appendix Table of Contents Specific Biological Raw Materials Animal 3502 Cell Standards for Production
  • 37药典 三部-2010 Contents of each monograph Ⅰ Prophylactic rabies vaccine for humans (Vero cells)
  • 259药典 三部-2010 Appendix Ⅹ XR Anti-human T cell immunoglobulin titer assay (lymphocytotoxicity test)
  • 165兽药典 三部-2015 Appendix Table of Contents Specific Biological Raw Material Animal 3504 Cell Monolayer Preparation Method
  • 39药典 三部-2010 Chapter Ⅰ Prophylactic Rabies Vaccine for Humans (Hamster Kidney Cells)
  • 9药典 三部-2010 General headings Preparation and verification procedures of animal cell matrix for production and verification of biological products
  • 172兽药典 三部-2015 Appendix Contents Reagents, Test Solution, Medium 3702 Preparation of Red Blood Cell Suspension
  • 农业部1719号公告-1-2012 Live swine fever vaccine (passage cell source) (new veterinary drug registration) (three types)
  • 159兽药典 三部-2015 Appendix Contents Biological Activity Potency Determination Method 3404 Erythrocyte Agglutination Inhibition Test Method
  • 25药典 三部-2010 Chapter Ⅰ Preventive Adsorbed Acellular DPT Combined Vaccine
  • 158兽药典 三部-2015 Appendix Contents Biological Activity Potency Determination Method 3403 Erythrocyte Agglutination Test Method
  • 118药典 三部-2010 Chapter II Therapeutic Recombinant Human Granulocyte Macrophage Stimulating Factor for Injection
  • 92药典 三部-2010 Chapter Ⅱ Therapeutic Anti-human T-cell Rabbit Immunoglobulin
  • 38药典 三部-2010 Contents of each monograph Ⅰ Preventive freeze-dried human rabies vaccine (Vero cells)
  • 43药典 三部-2010 Contents of each monograph Ⅰ Preventive recombinant hepatitis B vaccine (CHO cell)
  • 92兽药典 三部-2015 Contents of the text live vaccines swine fever live vaccines (cell source)
  • 93药典 三部-2010 Chapter II Therapeutic Recombinant Human Erythropoin for Injection (CHO Cell)
  • 91药典 三部-2010 Chapter Ⅱ Therapeutic anti-human T cell porcine immunoglobulin
  • 126药典 三部-2010 Chapter Ⅱ Therapeutic class Anti-human T cell CD3 mouse monoclonal antibody for injection
  • 49药典 三部-2010 Chapter Ⅰ Prevention of Rubella Live Attenuated Vaccine (Rabbit Kidney Cells)
  • 94药典 三部-2010 Chapter II Therapeutic Recombinant Human Erythropoin Injection (CHO Cell)

Professional Standard - Hygiene

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

  • JJG 714-1990 Verification Regulation of Blood Cell Analyzer
  • JJG 714-2012 Verification Regulation of Blood Cell Analyzers

国家药监局

  • YY/T 1825-2021 Guideline for measurement uncertainty evaluation of the certified values using the erythrocytes and leucocytes reference measurement procedures

National Health Commission of the People's Republic of China

  • WST 342:2011 Reference method for hematocrit determination

Association Francaise de Normalisation

  • NF EN 16418:2014 Paper and cardboard - Determination of the cytotoxic effect of aqueous extracts using a hepatoma cell line possessing metabolic enzymes (HepG2 cells)
  • NF Q03-111*NF EN 16418:2014 Paper and board - Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2)
  • NF S91-142:1988 Dental implants. Cytocompatibility. Study of cellular proliferation.
  • NF S91-145:1988 Dentistry. Dental implants. Cytocompatibility. Study of cells attachment and spreading on the biomaterial.
  • NF S91-143:1988 Dental implants. Cytocompatibility. Study of total cellular proteins.

KR-KS

  • KS M ISO 4590-2018 Rigid cellular plastics — Determination of the volume percentage of open cells and of closed cells

Korean Agency for Technology and Standards (KATS)

European Committee for Standardization (CEN)

  • EN 16418:2014 Paper and board - Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2)
  • EN ISO 18103:2015 Superfine woven wool fabric labelling - Requirements for Super S code definition (ISO 18103:2015)
  • EN ISO 4590:2016 Rigid cellular plastics - Determination of the volume percentage of open cells and of closed cells

SCC

  • DANSK DS/EN 16418:2014 Paper and board - Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2)
  • NS-EN 16418:2014 Paper and board — Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2)
  • DIN EN 16418 E:2012 Draft Document - Paper and board - Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2); German version prEN 16418:2012
  • MIL MIL-T-36153A-1977 TEST TUBE, HEMATOCRIT DETERMINATION, WINTROBE, DISPOSABLE (S/S BY A-A-54725)
  • BS 1335:1946 Specification for air depolarized primary cells
  • 12/30259424 DC BS EN 16418. Paper and board. Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2)
  • BS 1335:1968 Specification for air depolarized primary cells
  • DIN 58932-3 E:2016 Draft Document - Haematology - Determination of the concentration of blood corpuscles in blood - Part 3: Reference method for the determination of the concentration of erythrozytes; Text in German and English
  • CSA Z316.6-1995(R2000) Evaluation of Single Use Medical Sharps Containers for Biohazardous and Cytotoxic Waste

Spanish Association for Standardization (UNE)

  • UNE-EN 16418:2014 Paper and board - Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2)
  • UNE 53-201-1992 Plastics materials. Flexible foams of polyurethane. Determination of number of cells

German Institute for Standardization

  • DIN EN 16418:2014-07 Paper and board - Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2); German version EN 16418:2014
  • DIN EN 16418 E:2012-04 Paper and board - Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2)
  • DIN 58932-2:1998-06 Haematology - Determination of the concentration of blood corpuscles in blood - Part 2: Characteristic quantities for erythrocytes (erythrocyte indices)
  • DIN ISO 12772:2007-06 Laboratory glassware - Disposable microhaematocrit capillary tubes (ISO 12772:1997)
  • DIN 58932-2:1998 Haematology - Determination of the concentration of blood corpuscles in blood - Part 2: Characteristic quantities for erythrocytes (erythrocyte indices)
  • DIN EN 16418:2014 Paper and board - Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2); German version EN 16418:2014
  • DIN 58932-3:2023 Haematology - Determination of the concentration of blood corpuscles in blood - Part 3: Reference method for the determination of the concentration of erythrocytes; Text in German and English
  • DIN 58932-3:2024 Haematology - Determination of the concentration of blood corpuscles in blood - Part 3: Reference method for the determination of the concentration of erythrocytes; Text in German and English
  • DIN 58932-3:2023-07 Haematology - Determination of the concentration of blood corpuscles in blood - Part 3: Reference method for the determination of the concentration of erythrocytes; Text in German and English / Note: Date of issue 2023-06-02*Intended as replacement for...
  • DIN 58932-4:2003-07 Haematology - Determination of the concentration of blood corpuscles in blood - Part 4: Reference procedure for the determination of the concentration of leucocytes
  • DIN 58932-4:2003 Haematology - Determination of the concentration of blood corpuscles in blood - Part 4: Reference procedure for the determination of the concentration of leucocytes
  • DIN 58932-6 E:2021-02 Haematology - Determination of the concentration of blood corpuscles in blood - Part 6: Reference method for the determination of the concentration of CD4 positive lymphocytes
  • DIN 58932-6:2021-08 Haematology - Determination of the concentration of blood corpuscles in blood - Part 6: Reference method for the determination of the concentration of CD4 positive lymphocytes; Text in German and English

British Standards Institution (BSI)

  • BS EN 16418:2014 Paper and board. Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2)
  • BS ISO 12772:1997(1999) Laboratory Glassware — Disposable microhaematocrit capillary tubes
  • BS CWA 16336:2011 Superfine woven wool fabric labeling. Requirements for Super S code definition
  • BS ISO 20391-1:2018 Biotechnology. Cell counting. General guidance on cell counting methods
  • 23/30466937 DC BS ISO 24479 Biotechnology — Cellular morphological analysis — General requirements and considerations for cell morphometry to quantify cell morphological features
  • BS ISO 24479:2024 Biotechnology. Cellular morphological analysis. General requirements and considerations for cell morphometry to quantify cell morphological features

American National Standards Institute (ANSI)

HU-MSZT

  • MSZ 10192/10-1982 Check the definition of plastic, non-public cell number is clearly hard foam

American Society for Testing and Materials (ASTM)

  • ASTM E2526-08 Standard Test Method for Evaluation of Cytotoxicity of Nanoparticulate Materials in Porcine Kidney Cells and Human Hepatocarcinoma Cells
  • ASTM E734-80(2015) Standard Specification for Disposable Glass Blood Sample Capillary Tube (Microhematocrit)
  • ASTM E734-80(2005) Standard Specification for Disposable Glass Blood Sample Capillary Tube (Microhematocrit)
  • ASTM E734-80(2021) Standard Specification for Disposable Glass Blood Sample Capillary Tube (Microhematocrit)
  • ASTM E734-80(1999)e1 Standard Specification for Disposable Glass Blood Sample Capillary Tube (Microhematocrit)
  • ASTM F3368-19 Standard Guide for Cell Potency Assays for Cell Therapy and Tissue Engineered Products
  • ASTM F3354-19 Standard Guide for Evaluating Extracellular Matrix Decellularization Processes
  • ASTM D3576-20 Standard Test Method for Cell Size of Rigid Cellular Plastics
  • ASTM E3231-19 Standard Guide for Cell Culture Growth Assessment of Single-Use Material
  • ASTM F1027-86(2007) Standard Practice for Assessment of Tissue and Cell Compatibility of Orofacial Prosthetic Materials and Devices
  • ASTM E2526-22 Standard Test Method for Evaluation of Cytotoxicity of Nanoparticulate Materials in Porcine Kidney Cells and Human Hepatocarcinoma Cells
  • ASTM E1881-12 Standard Guide for Cell Culture Analysis with SIMS
  • ASTM D6226-21 Standard Test Method for Open Cell Content of Rigid Cellular Plastics
  • ASTM F895-11(2016) Standard Test Method for Agar Diffusion Cell Culture Screening for Cytotoxicity
  • ASTM F895-84(2001)e1 Standard Test Method for Agar Diffusion Cell Culture Screening for Cytotoxicity
  • ASTM F895-84(2006) Standard Test Method for Agar Diffusion Cell Culture Screening for Cytotoxicity
  • ASTM E2526-08(2013) Standard Test Method for Evaluation of Cytotoxicity of Nanoparticulate Materials in Porcine Kidney Cells and Human Hepatocarcinoma Cells
  • ASTM E1881-06 Standard Guide for Cell Culture Analysis with SIMS
  • ASTM F3088-22 Standard Practice for Use of a Centrifugation Method to Quantify/Study Cell-Material Adhesive Interactions
  • ASTM F895-84(2001) Standard Test Method for Agar Diffusion Cell Culture Screening for Cytotoxicity

GSO

  • OS GSO ISO 12772:2010 Laboratory glassware -- Disposable microhaematocrit capillary tubes
  • BH GSO ASTM E734:2022 Standard Specification for Disposable Glass Blood Sample Capillary Tube (Microhematocrit)
  • GSO ASTM E734:2021 Standard Specification for Disposable Glass Blood Sample Capillary Tube (Microhematocrit)
  • GSO ASTM F3206:2022 Standard Guide for Assessing Medical Device Cytocompatibility with Delivered Cellular Therapies
  • BH GSO ASTM F3206:2023 Standard Guide for Assessing Medical Device Cytocompatibility with Delivered Cellular Therapies

RU-GOST R

International Organization for Standardization (ISO)

  • ISO/DIS 24479:2023 Biotechnology — Cellular morphological analysis — General requirements and considerations for cell morphometry to quantify cell morphological features
  • ISO 18103:2015 Superfine woven wool fabric labelling - Requirements for Super S code definition

Military Standards (MIL-STD)

US-FCR

Canadian Standards Association (CSA)

  • CAN/CSA-Z900.2.5-2012 Lymphohematopoietic cells for transplantation (Second Edition; Update No 1: April 2013)