GB/T 16886.11-1997
Replaced
T/CNDIA 2-2025
Active
Group standards
T/CNDIA 2-2025 Clinical Application Guidelines for Platelet-Rich Plasma(PRP)in Wound Repair
T/CNDIA 2-2025 Clinical Application Guidelines for Platelet-Rich Plasma(PRP)in Wound Repair
Price:
$ 20.00
Basic Information
Standard Code:
T/CNDIA 2-2025
Standard Type:
Group standards
Standard Status:
Active
is_force_gb:
no
CCS Name:
Biological products and blood products
ICS Name:
Integrated medical equipment
Publish Date:
2025-10-30
Implement Date:
2025-11-10
Scope
This document specifies the terms and definitions, basic requirements, preparation methods, clinical applications, efficacy evaluation, and adverse reaction management of platelet-rich plasma (PRP) in wound repair. This document is applicable to clinical practices in all levels of medical institutions using PRP for wound repair treatment. This document specifies the terms and definitions, basic requirements, preparation methods, clinical applications, efficacy evaluation, and adverse reaction management of platelet-rich plasma (PRP) in wound repair.
Development Information
Related Standards
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
GB/T 16886.6-1997
Replaced
GB/T 16886.6-1997 Biological evaluation of medical devices—Part 6:Tests for local effects after implantation
GB/T 16886.1-2001
Replaced
GB/T 16886.1-2001 Biological evaluation of medical devices—Part 1:Evaluation and testing
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
GB/T 16886.7-2001
Replaced