FDA Device Intelligence
Home › IDMED › TOF-DS1

TOF-DS1

IDMED · Model TOF-DS1 · UDI-DI 03665023000467

KOI Prescription
1
510(k) clearances
48
Adverse events
1
Recalls
52
Facilities

Description

Disposable 3D-AMG hand sensor with stimulation electrodes

Recalls

DateFirmReason
2014-04-09GE Healthcare, LLCWhen the E-NMT-01 module is used in conjunction with the ElectroSensor, the Neuromuscular Transmission (NMT) values may indicate a deeper level of muscle relaxation than the actual

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data 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.