91E-SERIES 9120E UNKNOWN

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2020-03-02 for 91E-SERIES 9120E UNKNOWN manufactured by Getinge Disinfection Ab.

MAUDE Entry Details

Report Number9616031-2020-00009
MDR Report Key9774512
Report SourceCOMPANY REPRESENTATIVE,USER F
Date Received2020-03-02
Date of Report2020-03-02
Date Mfgr Received2020-02-05
Device Manufacturer Date2019-01-21
Date Added to Maude2020-03-02
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 ContactMR. DENNIS GENITO
Manufacturer StreetLJUNGADALSGATAN 11
Manufacturer CityVAXJO
Manufacturer CountryUS
Manufacturer G1GETINGE DISINFECTION AB
Manufacturer StreetLJUNGADALSGATAN 11
Manufacturer CityVAXJO
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand Name91E-SERIES
Generic NameDISINFECTOR, MEDICAL DEVICES
Product CodeMEC
Date Received2020-03-02
Model Number9120E
Catalog NumberUNKNOWN
Device AvailabilityY
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerGETINGE DISINFECTION AB
Manufacturer AddressLJUNGADALSGATAN 11 VAXJO US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-02

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