MAYO SCISSORS STR 170MM BC547R

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-08-13 for MAYO SCISSORS STR 170MM BC547R manufactured by Aesculap Ag.

MAUDE Entry Details

Report Number9610612-2019-00540
MDR Report Key8888365
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-08-13
Date of Report2019-08-13
Date Mfgr Received2019-07-15
Date Added to Maude2019-08-13
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
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
Manufacturer ContactMS KERSTIN ROTHWEILER
Manufacturer StreetPO BOX 40
Manufacturer CityTUTTLINGEN, 78501
Manufacturer CountryGM
Manufacturer Postal78501
Manufacturer G1AESCULAP AG
Manufacturer StreetPO BOX 40
Manufacturer CityTUTTLINGEN, 78501
Manufacturer CountryGM
Manufacturer Postal Code78501
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMAYO SCISSORS STR 170MM
Generic NameSURGICAL SCISSORS
Product CodeLRW
Date Received2019-08-13
Model NumberBC547R
Catalog NumberBC547R
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerAESCULAP AG
Manufacturer AddressPO BOX 40 TUTTLINGEN, 78501 GM 78501


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-08-13

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