HF-ELECTRODE, HOOK, 5 X 330 MM A6282

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,distri report with the FDA on 2020-03-23 for HF-ELECTRODE, HOOK, 5 X 330 MM A6282 manufactured by Olympus Winter & Ibe Gmbh.

MAUDE Entry Details

Report Number9610773-2020-00097
MDR Report Key9865630
Report SourceCOMPANY REPRESENTATIVE,DISTRI
Date Received2020-03-23
Date of Report2020-03-23
Date of Event2020-03-19
Date Mfgr Received2020-03-19
Device Manufacturer Date2016-06-10
Date Added to Maude2020-03-23
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. DANIEL WLADOW
Manufacturer StreetKUEHNSTRASSE 61
Manufacturer CityHAMBURG 22045
Manufacturer CountryGM
Manufacturer Postal22045
Manufacturer Phone4940669662
Manufacturer G1BOWA-ELECTRONIC GMBH & CO. KG
Manufacturer StreetHEINRICH-HERTZ-STRASSE 4-10
Manufacturer CityGOMARINGEN 72810
Manufacturer CountryGM
Manufacturer Postal Code72810
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameHF-ELECTRODE, HOOK, 5 X 330 MM
Generic NameHF ELECTRODES, RIGID
Product CodeGCJ
Date Received2020-03-23
Model NumberA6282
Catalog NumberA6282
Lot Number614818
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerOLYMPUS WINTER & IBE GMBH
Manufacturer AddressKUEHNSTRASSE 61 HAMBURG 22045 GM 22045


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-23

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