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SENTIO
Medos International Sàrl · Model 286202102 · UDI-DI 20705034534739
1
510(k) clearances
77
Adverse events (1 deaths)
2
Recalls
56
Facilities
Description
SENTIO MMG SENSORS 2 PACK WITH GROUND
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-06-23 | The Magstim Company Limited | Reports that manipulation of the cable which connects the pre-amplifier to the nerve monitor, and the cable which connects the pre-amplifier to the stimulator pod, may cause damage |
| 2020-06-10 | NuVasive Inc | The NVM5 EMG Module kit intended for intraoperative neurophysiologic monitoring during spinal surgery contains incorrect component, part number 1715945, SSEP harness instead of the |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.