ANTI-HUMAN GLOBULIN ANTI-IGG 804175100

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2020-02-03 for ANTI-HUMAN GLOBULIN ANTI-IGG 804175100 manufactured by Bio-rad Medical Diagnostics Gmbh.

MAUDE Entry Details

Report Number9610824-2020-00003
MDR Report Key9658894
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2020-02-03
Date of Report2020-02-03
Date of Event2019-12-06
Date Mfgr Received2020-01-09
Date Added to Maude2020-02-03
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 ContactMS MARTINA BENKERT
Manufacturer StreetINDUSTRIESTRASSE 1
Manufacturer CityDREIEICH, HESSEN 63303
Manufacturer CountryGM
Manufacturer Postal63303
Manufacturer G1BIO-RAD MEDICAL DIAGNOSTICS GMBH
Manufacturer StreetINDUSTRIESTRASSE 1
Manufacturer CityDREIEICH, 63303
Manufacturer CountryGM
Manufacturer Postal Code63303
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameANTI-HUMAN GLOBULIN ANTI-IGG
Generic NameANTI-HUMAN GLOBULIN, ANTI-IGG; 10ML
Product CodeKSZ
Date Received2020-02-03
Returned To Mfg2020-01-21
Catalog Number804175100
Lot Number8824120-04
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBIO-RAD MEDICAL DIAGNOSTICS GMBH
Manufacturer AddressINDUSTRIESTRASSE 1 DREIEICH, 63303 GM 63303


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-03

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