FDA Adverse Event Other Summary report: N

KARL STORZ

MDR report key: 3081052 · Received April 4, 2013

Report

Report Number
9610617-2013-00013
Event Type
Other
Date Received
April 4, 2013
Product Code
FCL
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

(B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
139535 KARL STORZ BIPOLAR CUTTING LOOP FCL

Patients

Seq Age Sex Outcome Treatment
1