WIRE,TONSIL,SNARE #7 MO2010-007

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1999-06-17 for WIRE,TONSIL,SNARE #7 MO2010-007 manufactured by Bauer & Haselbarth Gmbh.

MAUDE Entry Details

• Report Number: 6000008-1999-00006
• MDR Report Key: 230885
• Date Received: 1999-06-17
• Date of Report: 1999-06-16
• Date of Event: 1999-02-26
• Date Facility Aware: 1999-06-10
• Report Date: 1999-06-17
• Date Reported to FDA: 1999-06-17
• Date Reported to Mfgr: 1999-06-17
• Date Added to Maude: 1999-07-09
• Event Key: 0
• Report Source Code: Manufacturer report
• Manufacturer Link: Y
• Number of Patients in Event: 0
• Adverse Event Flag: 3
• Product Problem Flag: 0
• Reprocessed and Reused Flag: 0
• Reporter Occupation: RISK MANAGER
• Health Professional: 3
• Initial Report to FDA: 0
• Report to FDA: 3
• Event Location: 3
• Single Use: 3
• Previous Use Code: 3
• Event Type: 3
• Type of Report: 3

Device Details

• Brand Name: WIRE,TONSIL,SNARE #7
• Generic Name: INSTRUMENT
• Product Code: KBZ
• Date Received: 1999-06-17
• Model Number: MO2010-007
• Catalog Number: MO2010-007
• Lot Number: UNK
• ID Number: NA
• Device Availability: N
• Device Eval'ed by Mfgr: R
• Implant Flag: N
• Date Removed: A
• Device Sequence No: 1
• Device Event Key: 223835
• Manufacturer: BAUER & HASELBARTH GMBH
• Manufacturer Address: SAUERBRACH STRASSE 7 ELIERAU GM D-25479
• Baseline Brand Name: WIRE, TONSIL, SNARE #7
• Baseline Generic Name: INSTRUMENT
• Baseline Model No: MO2010-007
• Baseline Catalog No: MO2010-007
• Baseline ID: NA

Patients

Patient Number	Treatment	Outcome	Date
1	0	1. Other	1999-06-17