GB/T 46857.1-2025
医疗装备运维服务 第1部分:通用要求
Medical equipment operation and maintenance service一Part 1: General requirements
- 实施日期
- 2026-07-01
- ICS 分类
- 11.040.01
组合使用关键词、标准类型、状态与 ICS 分类,快速定位所需国家标准。
找到 22 条
GB/T 46857.1-2025
Medical equipment operation and maintenance service一Part 1: General requirements
GB/Z 130-2025
Post-market surveillance of medical devices for manufacturers
GB/Z 42217-2022
Medical device —Validation of software for medical device quality system
GB 9706.275-2022
Medical electrical equipment—Part 2-75: Particular requirements for the basic safety and essential performance of photodynamic therapy and photodynamic diagnosis equipment
GB/T 42062-2022
Medical devices—Application of risk management to medical devices
GB/T 42061-2022
Medical devices—Quality management systems—Requirements for regulatory purposes
GB/T 16886.4-2022
Biological evaluation of medical devices—Part 4: Selection of tests for interactions with blood
GB 9706.236-2021
Medical electrical equipment—Part 2-36: Particular requirements for the basic safety and essential performance of equipment for extracorporeally induced lithotripsy
GB 9706.260-2020
Medical electrical equipment—Part 2-60: Paticular requirments for the basic safety and essential performance of dental equipment
GB/T 16886.6-2015
Biological evaluation of medical devices—Part 6: Tests for local effects after implantation
GB/T 16886.2-2011
Biological evaluation of medical devices - Part 2: Animal welfare requirements
GB/T 16886.19-2011
Biological evaluation of medical devices - Part 19: Physico-chemical,morphological and topographical characterization of materials
GB/T 16886.18-2011
Biological evaluation of medical devices - Part 18: Chemical characterization of materials
GB/T 16886.11-2011
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity
GB/T 16886.1-2011
Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process
GB 9706.22-2003
Medical electricalequipment--Part 2: Particular requirements for the safety of equipment for extracorporeally induced lithotripsy
GB/T 16886.5-2003
Biological evaluation ofmedical devices--Part 5: Test for in vitro cytotoxicity
GB/T 16886.4-2003
Biological evaluation of medical devices--Part 4:Selection of tests for interactions with blood
GB/T 16886.15-2003
Biological evaluation of medical devices--Part 15:Identification and quantification of degradation products from metals and alloys
GB/T 16886.14-2003
Biological evaluation of medical devices--Part 14:Identification and quantification of degradation products from ceramics