T/CIET 584-2024 Active Group standards

T/CIET 584-2024 Medical molecular sieve oxygen concentrator equipment

Publish Date: 2024-07-31 Implement Date: 2024-07-31 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us

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Basic Information

Standard Code: T/CIET 584-2024

Standard Type: Group standards

Standard Status: Active

is_force_gb: no

CCS Name: -

ICS Name: Integrated medical equipment

Publish Date: 2024-07-31

Implement Date: 2024-07-31

Scope

Scope: This document specifies the abbreviations, working principles, basic requirements, usage conditions, technical requirements, test methods, inspection rules, marking, packaging, transportation, and storage of medical molecular sieve oxygen-generating equipment. This document applies to medical molecular sieve oxygen-generating equipment that supplies oxygen to multiple patients through a piping system, but does not apply to small-scale medical molecular sieve oxygen-generating equipment that directly supplies oxygen to patients. Main technical content: This document specifies the abbreviations, working principles, basic requirements, usage conditions, technical requirements, test methods, inspection rules, marking, packaging, transportation, and storage of medical molecular sieve oxygen-generating equipment. This document applies to medical molecular sieve oxygen-generating equipment that supplies oxygen to multiple patients through a piping system, but does not apply to small-scale medical molecular sieve oxygen-generating equipment that directly supplies oxygen to patients.

Development Information

Related Standards

GB/T 16886.11-1997 Replaced

GB/T 16886.11-1997 Biological evaluation of medical devices—Part 11:Tests for systemic toxicity

Publish Date: 1997-06-26

GB/T 16886.3-1997 Replaced

GB/T 16886.3-1997 Biological evaluation of medical devices—Part 3:Tests for genotoxicity, carcinogenicity and reproductive toxicity

Publish Date: 1997-06-26

GB/T 16886.6-1997 Replaced

GB/T 16886.6-1997 Biological evaluation of medical devices—Part 6:Tests for local effects after implantation

Publish Date: 1997-06-26

GB/T 16886.1-2001 Replaced

GB/T 16886.1-2001 Biological evaluation of medical devices—Part 1:Evaluation and testing

Publish Date: 2001-09-24

GB/T 16886.13-2001 Replaced

GB/T 16886.13-2001 Biological evaluation of medical devices—Part 13:Identification and quantification of degradation products from polymeric medical devices

Publish Date: 2001-09-24

GB/T 16886.7-2001 Replaced

GB/T 16886.7-2001 Biological evaluation of medical devices—Part 7:Ethylene oxide sterilization residuals

Publish Date: 2001-09-24