NASAL SCISSORS WT441500

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-06-28 for NASAL SCISSORS WT441500 manufactured by Olympus Winter & Ibe Gmbh.

MAUDE Entry Details

Report Number8743941
MDR Report Key8743941
Date Received2019-06-28
Date of Report2019-06-25
Date of Event2019-02-12
Report Date2019-06-25
Date Reported to FDA2019-06-25
Date Reported to Mfgr2019-06-28
Date Added to Maude2019-06-28
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationRISK MANAGER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNASAL SCISSORS
Generic NameSCISSORS, GENERAL, SURGICAL
Product CodeLRW
Date Received2019-06-28
Catalog NumberWT441500
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerOLYMPUS WINTER & IBE GMBH
Manufacturer Address136 TURNPIKE ROAD SOUTHBOROUGH MA 01772 US 01772


Patients

Patient NumberTreatmentOutcomeDate
10 2019-06-28

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.