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AAMI/ISO TI(R1549)9:2017 Biological evaluation of medical devices - Guidance on the conduct of biological evaluation within a risk management process
AAMI/ISO 17664:2017 Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices.
AAMI/ISO TIR80002-2:2017 Medical device software - Part 2: Validation of software for medical device quality systems
AAMI TIR71:2017 Guidance for logging of alarm system data
AAMI TIR59:2017 Integrating human factors into design controls
AAMI/ISO 11138-1:2017 Sterilization of health care products - Biological indicators - Part 1: General requirements
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