Full Description

This standard operating procedure provides a method for labeling medical devices with the "CE" marking. This procedure is suitable for all medical devices placed on the market or put into service within the European Economic Area (EEA) or wherever the Medical Device Directive (MDD) is applicable. Includes the attached form, "List of CE Marked Products Logsheet."

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Edition: 1 Published: 01/01/2005 Number of Pages: 3