NIM? 2.0 MAINFRAME 8252001IP

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-04-09 for NIM? 2.0 MAINFRAME 8252001IP manufactured by Medtronic Xomed Inc..

Event Text Entries

[141332893] The device was scrapped. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[141332894] A healthcare professional (hcp) reported that the device was not working. There was no known patient impact reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1045254-2019-00174
MDR Report Key8495503
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-04-09
Date of Report2019-04-09
Date Mfgr Received2018-02-23
Date Added to Maude2019-04-09
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 ContactURIZA SHUMS
Manufacturer Street6743 SOUTHPOINT DRIVE NORTH
Manufacturer CityJACKSONVILLE FL 32216
Manufacturer CountryUS
Manufacturer Postal32216
Manufacturer Phone9043328405
Manufacturer G1MEDTRONIC XOMED INC.
Manufacturer Street6743 SOUTHPOINT DR N
Manufacturer CityJACKSONVILLE FL 32216
Manufacturer CountryUS
Manufacturer Postal Code32216
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNIM? 2.0 MAINFRAME
Generic NameELECTROMYOGRAPH, DIAGNOSTIC
Product CodeIKN
Date Received2019-04-09
Returned To Mfg2018-03-28
Model Number8252001IP
Catalog Number8252001IP
Lot NumberNI
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerMEDTRONIC XOMED INC.
Manufacturer Address6743 SOUTHPOINT DR N JACKSONVILLE FL 32216 US 32216


Patients

Patient NumberTreatmentOutcomeDate
10 2019-04-09

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