T/SZMA 005-2026 Active Group standards

T/SZMA 005-2026 Basic configuration requirement for medical devices in tertiary public general hospitals

Publish Date: 2026-03-20 Implement Date: 2026-03-20 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/SZMA 005-2026

Standard Type: Group standards

Standard Status: Active

is_force_gb: no

CCS Name: Urban transportation facilities

ICS Name: Integrated medical equipment

Publish Date: 2026-03-20

Implement Date: 2026-03-20

Scope

This document stipulates the medical device configuration principles and overall requirements for tertiary-level public general hospitals, and specifies the main types and quantities of medical devices to be configured in clinical departments, medical technology departments, wards, outpatient (emergency) clinics, and triage counters. This document applies to the basic medical device configurations of newly built and renovated tertiary-level public general hospitals in Shenzhen City. Existing tertiary-level public general hospitals may refer to it for their medical device renewal work, and tertiary-level public specialized hospitals may use it as a reference. This document does not apply to the configuration of medical consumables, medical reagents, or medical devices specifically used for clinical trials, scientific research projects, or educational training purposes.

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