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.
[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
Report Number | 9610105-2014-00007 |
MDR Report Key | 3810793 |
Report Source | 01,05,06 |
Date Received | 2014-03-21 |
Date of Report | 2014-01-17 |
Date of Event | 2014-01-17 |
Date Mfgr Received | 2014-01-17 |
Device Manufacturer Date | 2013-09-01 |
Date Added to Maude | 2014-06-02 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Manufacturer Contact | JOY SONSALLA |
Manufacturer Street | 3000 N. GRANDVIEW BLVD. W450 |
Manufacturer City | WAUKESHA WI 53188 |
Manufacturer Country | US |
Manufacturer Postal | 53188 |
Manufacturer Phone | 2625482661 |
Manufacturer G1 | GE HEALTHCARE |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | S/5 NEUROMUSCULAR TRANSMISSION MODULE, E-NMT |
Generic Name | STIMULATOR, NERVE, PERIPHERAL, ELECT |
Product Code | KOI |
Date Received | 2014-03-21 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | GE HEALTHCARE FINLAND OY |
Manufacturer Address | HELSINKI FI |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2014-03-21 |