CARB-BITE MAYO-HEGAR NEEDLEHOLDER 7 AR 200-18-61 121-140

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor report with the FDA on 2020-01-17 for CARB-BITE MAYO-HEGAR NEEDLEHOLDER 7 AR 200-18-61 121-140 manufactured by Geomed Medizin-technik Gmbh & Co. Kg.

MAUDE Entry Details

Report Number8010168-2020-00001
MDR Report Key9600196
Report SourceDISTRIBUTOR
Date Received2020-01-17
Date of Report2020-01-17
Date of Event2019-09-19
Date Mfgr Received2019-12-19
Date Added to Maude2020-01-17
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 ContactHANNO HAUG
Manufacturer StreetLUDWIGSTALER STRASSE 27
Manufacturer CityTUTTLINGEN, BW 78532
Manufacturer CountryGM
Manufacturer Postal78532
Manufacturer G1GEOMED MEDIZIN-TECHNIK GMBH & CO. KG
Manufacturer StreetLUDWIGSTALER STRASSE 27
Manufacturer CityTUTTLINGEN, 78532
Manufacturer CountryGM
Manufacturer Postal Code78532
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCARB-BITE MAYO-HEGAR NEEDLEHOLDER 7
Generic NameCARDIOVASCULAR NEEDLEHOLDER
Product CodeDWS
Date Received2020-01-17
Model NumberAR 200-18-61
Catalog Number121-140
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerGEOMED MEDIZIN-TECHNIK GMBH & CO. KG
Manufacturer AddressLUDWIGSTALER STRASSE 27 TUTTLINGEN, 78532 GM 78532


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-17

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