CONFIRM ANTI-SYNAPTOPHYSIN (SP11) RABBIT 05479304001

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2020-03-18 for CONFIRM ANTI-SYNAPTOPHYSIN (SP11) RABBIT 05479304001 manufactured by Ventana Medical Systems, Inc..

MAUDE Entry Details

Report Number2028492-2020-00003
MDR Report Key9850188
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2020-03-18
Date of Report2020-03-18
Date of Event2020-02-20
Date Mfgr Received2020-02-20
Device Manufacturer Date2019-06-05
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
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactNA STACIE-ANN CREIGHTON
Manufacturer Street1910 E INNOVATION PARK DR NA
Manufacturer CityTUSCON AZ 85755
Manufacturer CountryUS
Manufacturer Postal85755
Manufacturer Phone9082537112
Manufacturer G1NA
Manufacturer StreetNA NA
Manufacturer CityNA
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameCONFIRM ANTI-SYNAPTOPHYSIN (SP11) RABBIT
Generic NameIMMUNOHISTOCHEMISTRY REAGENTS AND KITS
Product CodeNJT
Date Received2020-03-18
Model NumberNA
Catalog Number05479304001
Lot NumberF11948
OperatorHEALTH PROFESSIONAL
Device Availability*
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerVENTANA MEDICAL SYSTEMS, INC.
Manufacturer Address1910 E INNOVATION PARK DR TUCSON AZ 85755 US 85755


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-03-18

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