NOIR BABY-METZ SCISSORS CVD 145MM BC259B

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 2019-08-27 for NOIR BABY-METZ SCISSORS CVD 145MM BC259B manufactured by Aesculap Ag.

MAUDE Entry Details

Report Number9610612-2019-00583
MDR Report Key8935741
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-08-27
Date of Report2019-10-09
Date of Event2019-07-25
Date Mfgr Received2019-07-29
Device Manufacturer Date2016-01-24
Date Added to Maude2019-08-27
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
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 NameNOIR BABY-METZ SCISSORS CVD 145MM
Generic NameDUROTIP SCISSORS
Product CodeLRW
Date Received2019-08-27
Returned To Mfg2019-08-16
Model NumberBC259B
Catalog NumberBC259B
Lot Number4507294698
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerAESCULAP AG
Manufacturer AddressPO BOX 40 TUTTLINGEN, 78501 GM 78501


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-08-27

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