HETTICH EBA 21 1004

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-01-30 for HETTICH EBA 21 1004 manufactured by Andreas Hettich Gmbh & Co. Kg.

MAUDE Entry Details

Report Number3005990076-2020-00002
MDR Report Key9647956
Report SourceHEALTH PROFESSIONAL
Date Received2020-01-30
Date of Report2020-01-30
Date of Event2018-11-29
Report Date2018-12-10
Date Reported to Mfgr2018-12-10
Date Mfgr Received2018-12-10
Device Manufacturer Date2014-02-24
Date Added to Maude2020-01-30
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 ContactMR. JOHANN GIEBELHAUS
Manufacturer StreetFOEHRENSTR. 12
Manufacturer CityTUTTLINGEN, BADEN-WUERTTEMBERG 78532
Manufacturer CountryGM
Manufacturer Postal78532
Manufacturer G1ANDREAS HETTICH GMBH & CO. KG
Manufacturer StreetFOEHRENSTR. 12
Manufacturer CityTUTTLINGEN, BADEN-WUERTTEMBERG 78532
Manufacturer CountryGM
Manufacturer Postal Code78532
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameHETTICH
Generic NameEBA 21
Product CodeJQC
Date Received2020-01-30
Returned To Mfg2018-12-12
Model NumberEBA 21
Catalog Number1004
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Age4 YR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerANDREAS HETTICH GMBH & CO. KG
Manufacturer AddressFOEHRENSTR. 12 TUTTLINGEN, BADEN-WUERTTEMBERG 78532 GM 78532


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-30

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