GB/T 16886.11-1997
Replaced
T/CAMDI 123.9-2023
Active
Group standards
T/CAMDI 123.9-2023 Medical rehabilitation robotics - Part 9: Risk evaluation methods
T/CAMDI 123.9-2023 Medical rehabilitation robotics - Part 9: Risk evaluation methods
Price:
$ 20.00
Basic Information
Standard Code:
T/CAMDI 123.9-2023
Standard Type:
Group standards
Standard Status:
Active
is_force_gb:
no
CCS Name:
-
ICS Name:
Integrated medical equipment
Publish Date:
2023-12-28
Implement Date:
2023-12-31
Pages:
11 pages
Scope
Main technical content: This document specifies the risk assessment methods, risk assessment procedures, and document requirements for the life cycle of medical rehabilitation robots, and provides examples of hazard identification, risk assessment, and risk control for medical rehabilitation robots. This document is applicable to the risk assessment of medical rehabilitation robots. It is not applicable to the risk assessment of industrial robots, personal/household service robots, public service robots, and special robots.
Development Information
Same series standard
T/CAMDI 123.1-2023 Medical rehabilitation robot - Part 1: Determination of dynamic torque fluctuation coefficient
T/CAMDI 123.2-2023 Medical rehabilitation robot - Part 2: Test method for expected lifetime of power modules
T/CAMDI 123.3-2023 Medical rehabilitation robot - Part 3: Test method for spasticity sensitivity
T/CAMDI 123.4-2023 Medical rehabilitation robot - Part 4: Method for testing the expected lifespan of the power module output interface
T/CAMDI 123.5-2023 Medical rehabilitation robot - Part 5: Method for aging testing of drag chain cables
T/CAMDI 123.6-2023 Medical rehabilitation robot - Part 6: Test method for stall torque of power modules
T/CAMDI 123.7-2023 Medical rehabilitation robot - Part 7: Life acceleration test method
T/CAMDI 123.8-2023 Medical rehabilitation robot - Part 8: Measurement of noise
T/CAMDI 123.10-2023 Medical rehabilitation robotics - Part 10: Safety evaluation method for portable power lithium batteries
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