NIM? 3.0 MAINFRAME INTERNATIONAL 8253002

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 2020-02-19 for NIM? 3.0 MAINFRAME INTERNATIONAL 8253002 manufactured by Medtronic Xomed Inc..

Event Text Entries

[182002454] Other relevant device(s) are: product id: 8253200, serial/lot #: (b)(4), udi#: (b)(4). Analysis of the mainframe found that the customers reason for return had been confirmed, the nim failed the impedance measurement function test, stim 1 return is off. The latest software version was installed. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[182002455] A healthcare professional (hcp) reported that the mainframe/interface was not working. There was no patient impact.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1045254-2020-00095
MDR Report Key9726997
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-02-19
Date of Report2020-03-17
Date of Event2020-01-28
Date Mfgr Received2020-02-24
Device Manufacturer Date2013-01-16
Date Added to Maude2020-02-19
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 ContactCHRISTY CAIN
Manufacturer Street6743 SOUTHPOINT DRIVE NORTH
Manufacturer CityJACKSONVILLE FL 32216
Manufacturer CountryUS
Manufacturer Postal32216
Manufacturer Phone9043328353
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? 3.0 MAINFRAME INTERNATIONAL
Generic NameSTIMULATOR, NERVE
Product CodeETN
Date Received2020-02-19
Returned To Mfg2020-02-10
Model Number8253002
Catalog Number8253002
Lot Number206517161
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
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 2020-02-19

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