86-SERIES 8668 S-86682003-CTOM

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 2020-02-11 for 86-SERIES 8668 S-86682003-CTOM manufactured by Getinge Disinfection Ab.

MAUDE Entry Details

Report Number9616031-2020-00006
MDR Report Key9693607
Report SourceCOMPANY REPRESENTATIVE,USER F
Date Received2020-02-11
Date of Report2020-02-11
Date of Event2020-01-20
Date Mfgr Received2020-01-20
Device Manufacturer Date2008-08-12
Date Added to Maude2020-02-11
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 Name86-SERIES
Generic NameDISINFECTOR, MEDICAL DEVICES
Product CodeMEC
Date Received2020-02-11
Model Number8668
Catalog NumberS-86682003-CTOM
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 2020-02-11

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