This American National Standard specifies a procedure by which a manufacturer can identify thehazards associated with medical devices and their accessories (including in vitro diagnosticmedical devices), estimate and evaluate the risks, control these risks, and monitor theeffectiveness of the control.
- Published:
- 10/16/2000
- ANSI:
- ANSI Approved
- Number of Pages:
- 41
- File Size:
- 1 file , 190 KB
- Note:
- This product is unavailable in Russia, Ukraine, Belarus
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