GB/T 16886.11-1997
Replaced
T/CAMDI 029-2024
Active
Group standards
T/CAMDI 029-2024 Additive manufacturing and personalized medical device requirements for interdisciplinary interaction
T/CAMDI 029-2024 Additive manufacturing and personalized medical device requirements for interdisciplinary interaction
Price:
$ 20.00
Basic Information
Standard Code:
T/CAMDI 029-2024
Standard Type:
Group standards
Standard Status:
Active
is_force_gb:
no
CCS Name:
-
ICS Name:
Integrated medical equipment
Publish Date:
2024-04-23
Implement Date:
2024-05-01
Pages:
16 pages
Scope
Main technical content: This document specifies the general requirements for the interaction between medical engineers and additive manufacturing of personalized medical devices, including general requirements, basic processes, design and development, production, delivery, judgment, acceptance, use follow-up and feedback. This document is applicable to additive manufacturing of personalized medical devices such as bones, joints, and oral hard tissues, as well as related tools.
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