Mdr report key: 70854
Report Number: 2647580-1997-00157
Report Source Code: M
Manufacturer Link Flag: Y
Adverse Event Flag: Y
Product Problem Flag: N
Health Professional: Y
Initial Report to FDA: N
Date facility Aware: 1997-01-15
Event Location: 001
Device date of Manufacture: 1996-01-06
Single Use Flag: Y
Previous Use Code: I
Event Type: IN
Type of Report: I,F
Source Type: 01,05,06,07
Reporter Country Code: FR
Summary Report: N
NOE Summarized: 1
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