FLEXIBLE BIOPSY FORCEPS 829.07

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2019-11-22 for FLEXIBLE BIOPSY FORCEPS 829.07 manufactured by Richard Wolf Gmbh.

MAUDE Entry Details

Report Number1418479-2019-00055
MDR Report Key9365747
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2019-11-22
Date of Report2019-10-23
Date Facility Aware2019-10-23
Report Date2019-11-22
Date Reported to FDA2019-11-22
Date Reported to Mfgr2019-11-22
Date Mfgr Received2019-11-07
Device Manufacturer Date2019-03-06
Date Added to Maude2019-11-22
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. OLIVER EHRLICH
Manufacturer StreetPFORZHEIMER STREET 32
Manufacturer CityKNITTLINGEN, 75438
Manufacturer CountryGM
Manufacturer Postal75438
Manufacturer G1RICHARD WOLF GMBH
Manufacturer StreetPFORZHEIMER STREET 32
Manufacturer CityKNITTLINGEN, 75438
Manufacturer CountryGM
Manufacturer Postal Code75438
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameFLEXIBLE BIOPSY FORCEPS
Generic NameFLEXIBLE BIOPSY FORCEPS
Product CodeFCL
Date Received2019-11-22
Returned To Mfg2019-10-25
Model Number829.07
Catalog Number829.07
Lot Number4500268255
Device AvailabilityR
Device Age8 MO
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerRICHARD WOLF GMBH
Manufacturer AddressPFORZHEIMER STREET 32 KNITTLINGEN, 75438 GM 75438


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-11-22

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