GB/T 16886.11-1997
Replaced
T/CAMDI 093-2022
Active
Group standards
T/CAMDI 093-2022 Medical additive manufacturing, control and validation requirements for photo-curing forming process
T/CAMDI 093-2022 Medical additive manufacturing, control and validation requirements for photo-curing forming process
Price:
$ 20.00
Basic Information
Standard Code:
T/CAMDI 093-2022
Standard Type:
Group standards
Standard Status:
Active
is_force_gb:
no
CCS Name:
-
ICS Name:
Integrated medical equipment
Publish Date:
2022-12-30
Implement Date:
2023-01-01
Pages:
12 pages
Scope
Main technical content: This document specifies the general requirements for routine control and process confirmation of medical additive manufacturing photocuring molding processes. This document is applicable to stereo lithography apparatus (SLA), digital light processing (DLP), and masked stereo lithography apparatus (MSLA) technologies. When other photocuring molding technologies are involved, the relevant content of this document can be used as a reference, but its applicability should be judged by the users of this document.
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