MOBILE CART CAMERA 10295

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-03-09 for MOBILE CART CAMERA 10295 manufactured by Natus Medical Incorporated.

MAUDE Entry Details

Report Number9612330-2020-00003
MDR Report Key9805143
Report SourceHEALTH PROFESSIONAL
Date Received2020-03-09
Date of Report2020-03-09
Date Added to Maude2020-03-09
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 ContactMICHELLE GREANEY
Manufacturer StreetIDA BUSINESS PARK GORT
Manufacturer CityGALWAY, H91PD92
Manufacturer CountryEI
Manufacturer PostalH91PD92
Manufacturer G1NATUS MEDICAL INCORPORATED
Manufacturer StreetDBA EXCEL-TECH LTD. (XLTEK) 2568 BRISTOL CIRCLE
Manufacturer CityOAKVILLE, ONTARIO L6H 5S1
Manufacturer CountryCA
Manufacturer Postal CodeL6H 5S1
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMOBILE CART CAMERA
Generic NameMOBILE CART CAMERA
Product CodeFTT
Date Received2020-03-09
Model Number10295
OperatorHEALTH PROFESSIONAL
Device Availability*
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerNATUS MEDICAL INCORPORATED
Manufacturer AddressDBA EXCEL-TECH LTD. (XLTEK) 2568 BRISTOL CIRCLE OAKVILLE, ONTARIOS L6H 5S1 CA L6H 5S1


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-09

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