OLYMPIC BILI-BASSINET 58110

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2020-01-16 for OLYMPIC BILI-BASSINET 58110 manufactured by Natus Medical Incorporated.

MAUDE Entry Details

Report Number3018859-2020-00001
MDR Report Key9598506
Report SourceUSER FACILITY
Date Received2020-01-16
Date of Report2019-12-31
Date of Event2019-12-31
Date Mfgr Received2019-12-31
Date Added to Maude2020-01-16
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 ContactMR. MONTHER ABUSHABAN
Manufacturer Street5900 1ST AVENUE SOUTH
Manufacturer CitySEATTLE WA 98108
Manufacturer CountryUS
Manufacturer Postal98108
Manufacturer Phone8582602522
Manufacturer G1NATUS MEDICAL INCORPORATED
Manufacturer Street5900 1ST AVENUE SOUTH
Manufacturer CitySEATTLE WA 98108
Manufacturer CountryUS
Manufacturer Postal Code98108
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameOLYMPIC BILI-BASSINET
Generic NameBILI-BASSINET MODEL 10
Product CodeLBI
Date Received2020-01-16
Model Number58110
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerNATUS MEDICAL INCORPORATED
Manufacturer Address5900 1ST AVENUE SOUTH SEATTLE WA 98108 US 98108


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-01-16

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