1053, AURICAL FREEFIT 8-62-45300

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 2019-09-04 for 1053, AURICAL FREEFIT 8-62-45300 manufactured by Natus Medical Denmark (gn Otometrics).

MAUDE Entry Details

Report Number9612197-2019-00015
MDR Report Key8960010
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2019-09-04
Date of Report2019-11-27
Date of Event2019-08-14
Date Mfgr Received2019-08-14
Date Added to Maude2019-09-04
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 ContactMISS LOUISE CALLANAN
Manufacturer StreetIDA BUSINESS PARK GORT
Manufacturer CityGALWAY, CONNAUGHT H91PD92
Manufacturer CountryEI
Manufacturer PostalH91PD92
Manufacturer G1NATUS MEDICAL DENMARK (GN OTOMETRICS)
Manufacturer StreetHOERSKAETTEN 9,
Manufacturer CityTAASTRUP, 2630
Manufacturer CountryDA
Manufacturer Postal Code2630
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand Name1053, AURICAL FREEFIT
Generic Name1053, AURICAL FREEFIT
Product CodeETW
Date Received2019-09-04
Model Number8-62-45300
Catalog Number8-62-45300
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerNATUS MEDICAL DENMARK (GN OTOMETRICS)
Manufacturer AddressHOERSKAETTEN 9, TAASTRUP, 2630 DA 2630


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-09-04

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