Published on

January 25, 2022

Last updated on

March 29, 2022

December 2021 Regulatory Roundup for Medical Device Mandatory Standards

December 2021 Regulatory Roundup for Medical Device Mandatory Standards

On December 14, 2021, the NMPA (National Medical Products Administration) published a draft list of 76 standards associated to GB 9706.1-2020 to solicit public comments. The GB 9706.1-2020 medical electrical equipment Part 1: General requirements for basic safety and basic performance was issued on April 9, 2020, and will be implemented on May 1, 2023. Aside from GB 9706.1-2020 itself, the draft list consists of 68 specialized standards and 7 collateral standards. According to the implementation measures proposed by the NMPA,

  • The date of implementation for GB 9706.1-2020 and its collateral standards will be May 1, 2023.
  • Specialized standards under GB9706.1-2020 are indicated as standards with special requirements which will be further clarified when the draft is finalized.

On December 1, 2021, the Standardization Administration approved and issued (No.15-2021) 8 national standards for medical devices:

  1. GB 9706.202-2021 Medical electrical equipment - Part 2-2: Particular requirements for basic safety and basic performance of high frequency surgical equipment and high frequency accessories
  2. GB 9706.213-2021 Medical electrical equipment - Part 2-13: Particular requirements for the basic safety and basic performance of anesthesia workstations
  3. GB 9706.218-2021 Medical electrical equipment - Part 2-18: Particular requirements for the basic safety and basic performance of endoscopic equipment
  4. GB 9706.224-2021 Medical electrical equipment - Part 2-24: Particular requirements for the basic safety and basic performance of infusion pumps and infusion controllers
  5. GB 9706.225-2021 Medical electrical equipment - Part 2-25: Particular requirements for the basic safety and basic performance of electrocardiographs
  6. GB 9706.236-2021 Medical electrical equipment - Part 2-36: Particular requirements for the basic safety and basic performance of extracorporeal lithotripsy equipment
  7. GB 11236-2021 Technical requirements and test methods of copper IUD
  8. GB 14232.4-2021 Plastic bag containers for human blood and blood components - Part 4: single blood bag system with special components

On December 10, 2021, the NMPA approved and issued (No.144-2021) 19 industry standards for medical devices:

  1. YY/T 1747-2021 Neurovascular implants Intracranial artery stents
  2. YY/T 1784-2021 Blood gas analyzer
  3. YY/T 1789.2-2021 In Vitro Diagnostic Test System Performance Evaluation Method Part 2: Accuracy
  4. YY/T 1791-2021 Hepatitis B virus e antibody detection kit (luminescence immunoassay)
  5. YY/T 1801-2021 Fetal chromosome aneuploidy trisomy 21, trisomy 18 and trisomy 13 detection kit (high-throughput sequencing method)
  6. YY/T 1820-2021 Specific antinuclear antibody IgG detection kit (Western blotting)
  7. YY/T 1824-2021 EB virus nucleic acid detection kit (fluorescence PCR method)
  8. YY/T 1825-2021 Red blood cell and white blood cell count reference measurement procedure fixed value result measurement uncertainty evaluation guide
  9. YY/T 1826-2021 Group B Streptococcus Nucleic Acid Detection Kit (Fluorescence PCR Method)
  10. YY/T 1828-2021 Anti-Mullerian hormone determination kit (chemiluminescence immunoassay)
  11. YY/T 1831-2021 Syphilis spirochete antibody detection kit (immunochromatographic method)
  12. YY/T 1836-2021 Respiratory virus multiple nucleic acid detection kit
  13. YY/T 0500-2021 Cardiovascular implants: Vascular prostheses – Tubular vascular grafts and vascular patches
  14. YY/T 0647-2021 Passive surgical implants: Specific requirements for breast implants
  15. YY/T 0701-2021 Calibrator for blood analyzer
  16. YY/T 1160-2021 Carcinoembryonic Antigen (CEA) Assay Kit
  17. YY/T 1164-2021 Human chorionic gonadotropin (HCG) detection kit (colloidal gold immunochromatographic method)
  18. YY/T 1180-2021 Human Leukocyte Antigen (HLA) Genotyping Test Kit
  19. YY/T 1204-2021 Kit for determination of total bile acid

The code name of the mandatory national standard is "GB", and the recommended national standard is "GB/T". The code name of the mandatory industry standard is "YY", and the code name of the recommended industry standard is "YY/T". Contact Cisema if you would like to learn more about the compliance requirements for your medical product in China.

By Alice Liu and Jacky Li.

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