S/5 NEUROMUSCULAR TRANSMISSION MODULE, E-NMT

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05,06 report with the FDA on 2014-03-21 for S/5 NEUROMUSCULAR TRANSMISSION MODULE, E-NMT manufactured by Ge Healthcare Finland Oy.

Event Text Entries

[15881456] Pt date not currently available. A f/u report will be submitted when the investigation is complete.
Patient Sequence No: 1, Text Type: N, H10


[15934244] The customer reported the e-nmt-01 module provided inaccurate readings when being used with an electrosensor. There was no reported pt injury associated with this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9610105-2014-00007
MDR Report Key3810793
Report Source01,05,06
Date Received2014-03-21
Date of Report2014-01-17
Date of Event2014-01-17
Date Mfgr Received2014-01-17
Device Manufacturer Date2013-09-01
Date Added to Maude2014-06-02
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 FDA0
Event Location0
Manufacturer ContactJOY SONSALLA
Manufacturer Street3000 N. GRANDVIEW BLVD. W450
Manufacturer CityWAUKESHA WI 53188
Manufacturer CountryUS
Manufacturer Postal53188
Manufacturer Phone2625482661
Manufacturer G1GE HEALTHCARE
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameS/5 NEUROMUSCULAR TRANSMISSION MODULE, E-NMT
Generic NameSTIMULATOR, NERVE, PERIPHERAL, ELECT
Product CodeKOI
Date Received2014-03-21
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerGE HEALTHCARE FINLAND OY
Manufacturer AddressHELSINKI FI


Patients

Patient NumberTreatmentOutcomeDate
10 2014-03-21

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