T/ZGCIT 014-2024 Active Group standards

T/ZGCIT 014-2024 Guidelines for the clinical application of biodegradable composite bone cement for the treatment of osteoporotic vertebral compression fractures

Publish Date: 2024-12-30 Implement Date: 2024-12-30 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/ZGCIT 014-2024

Standard Type: Group standards

Standard Status: Active

is_force_gb: no

CCS Name: -

ICS Name: Integrated medical equipment

Publish Date: 2024-12-30

Implement Date: 2024-12-30

Scope

Scope: This document specifies the indications and contraindications for the treatment of osteoporotic vertebral compression fractures with degradable composite bone cement, as well as the requirements for institutions and personnel, the treatment process, follow-up, and the monitoring of adverse reactions. This document applies to the treatment of patients with osteoporotic vertebral compression fractures using degradable composite bone cement in the orthopedic departments of general hospitals. Main technical content: This document specifies the indications and contraindications for the treatment of osteoporotic vertebral compression fractures with degradable composite bone cement, as well as the requirements for institutions and personnel, the treatment process, follow-up, and the monitoring of adverse reactions.

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