APPLICATION INSTRUMENT FO STERNAL ZIPFIX 03.501.080

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 2020-01-21 for APPLICATION INSTRUMENT FO STERNAL ZIPFIX 03.501.080 manufactured by Oberdorf Synthes Produktions Gmbh.

MAUDE Entry Details

Report Number8030965-2020-00532
MDR Report Key9613542
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-01-21
Date of Report2019-12-27
Date of Event2019-12-26
Date Mfgr Received2020-02-04
Device Manufacturer Date2016-03-31
Date Added to Maude2020-01-21
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 ContactKARA DITTY-BOVARD
Manufacturer StreetEIMATTSTRASSE 3
Manufacturer CityOBERDORF 4436
Manufacturer CountrySZ
Manufacturer Postal4436
Manufacturer Phone6103142063
Manufacturer G1WERK H
Manufacturer StreetIM BIFANG 6
Manufacturer CityHAEGENDORF 4614
Manufacturer CountrySZ
Manufacturer Postal Code4614
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameAPPLICATION INSTRUMENT FO STERNAL ZIPFIX
Generic NameAPPLIANCE,FIXATION DEVICE, PROXIMAL FEMUR
Product CodeJDO
Date Received2020-01-21
Returned To Mfg2020-01-13
Catalog Number03.501.080
Lot Number9790420
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerOBERDORF SYNTHES PRODUKTIONS GMBH
Manufacturer AddressEIMATTSTRASSE 3 OBERDORF 4436 SZ 4436


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-21

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