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,health report with the FDA on 2016-05-16 for NIM? 2.0 MAINFRAME 8252001IP manufactured by Medtronic Xomed Inc..

Event Text Entries

[45221397] Concomitant medical device: 8252800: interface 8252800 response 2. 0 increment, s/n (b)(4), lot 56523600, manufactured: 06/16/2008. Product evaluation: analysis results not available; no devices returned for evaluation.
Patient Sequence No: 1, Text Type: N, H10


[45221398] It was reported that the "old system is unreliable and increasingly not user-friendly. Sometimes they are visibly looking at the nerve and seeing it and not seeing in on the monitor with stimulation. " there was no patient impact.
Patient Sequence No: 1, Text Type: D, B5


[102520541] If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1045254-2016-00147
MDR Report Key5656206
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2016-05-16
Date of Report2016-04-19
Date Mfgr Received2016-04-19
Device Manufacturer Date2008-06-13
Date Added to Maude2016-05-16
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 ALFORD
Manufacturer Street6743 SOUTHPOINT DRIVE NORTH
Manufacturer CityJACKSONVILLE FL 32216
Manufacturer CountryUS
Manufacturer Postal32216
Manufacturer Phone9043328197
Manufacturer G1MEDTRONIC XOMED INC.
Manufacturer Street6743 SOUTHPOINT DR NORTH
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 Received2016-05-16
Model Number8252001IP
Catalog Number8252001IP
Lot Number56541200
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerMEDTRONIC XOMED INC.
Manufacturer Address6743 SOUTHPOINT DR NORTH JACKSONVILLE FL 32216 US 32216


Patients

Patient NumberTreatmentOutcomeDate
10 2016-05-16

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.