TRIAL INSERTER SH CONNECTION TFT20101

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 2020-03-18 for TRIAL INSERTER SH CONNECTION TFT20101 manufactured by Eit Emerging Implant Technologies Gmbh.

MAUDE Entry Details

Report Number3013730328-2020-00013
MDR Report Key9847408
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-18
Date of Report2020-02-20
Date of Event2020-02-13
Date Mfgr Received2020-02-20
Date Added to Maude2020-03-18
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 ContactKARA DITTY-BOVARD
Manufacturer StreetEISENBAHNSTRASSE 84
Manufacturer CityWURMLINGEN D-78573
Manufacturer CountryGM
Manufacturer PostalD-78573
Manufacturer Phone6103142063
Manufacturer G1EIT EMERGING IMPLANT TECHNOLOGIES GMBH
Manufacturer CountryGM
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTRIAL INSERTER SH CONNECTION
Generic NameINTERVERTEBAL FUSION DEVICE W/BONE GRAFT, LUMBAR
Product CodeMAX
Date Received2020-03-18
Model NumberTFT20101
Catalog NumberTFT20101
Lot NumberE18DI0306
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerEIT EMERGING IMPLANT TECHNOLOGIES GMBH
Manufacturer AddressEISENBAHNSTRASSE 84 WURMLINGEN DE


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-18

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