Specifies a procedure to investigate, using available information, the safety of medical devices by identifying hazards and estimating the risks associated with the device (risk analysis). This Standrad applies to medical devices (excluding in-vitro diagnostic medical devices) manufactured utilizing animal tissue or products derived from animal tissue, which are non-viable or have been rendererd non-viable.
AS EN 12442.1-2003
Original price was: $122.10.$61.00Current price is: $61.00.
Animal tissues and their derivatives utilized in the manufacture of medical devices, Part 1: Analysis and management of risk
Standards Australia , 01/01/2003
Pages: 17
