Home › Device types › KOI
Stimulator, Nerve, Peripheral, Electric
FDA product code KOI · Class 2 · Anesthesiology
143
Registered devices
48
Adverse events
1
Recalls
29
510(k) clearances
Devices with this code
NA — GE Medical Systems Information Technologies, Inc.TOF — IDMEDCARESCAPE B450 — GE Healthcare Finland OyNMT cable — Philips Medizin Systeme Böblingen GmbHEye adapter TOF3D — MIPM Mammendorfer Institut für Physik und Medizin GmbHHalyard — Avanos Medical, Inc.WiTOF — IDMEDNA — GE Healthcare Finland OyWiTOF — IDMEDTetraSens Pediatric — Senzime AB (Publ.)IV-pole holder TOF3D Variant B - Standard — MIPM Mammendorfer Institut für Physik und Medizin GmbHWiTOF — IDMEDTOF-DEMO_F — IDMEDTOF3D - Neuromuscular Transmission Monitor — MIPM Mammendorfer Institut für Physik und Medizin GmbHNA — GE Medical Systems Information Technologies, Inc.CARESCAPE — GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC.CARESCAPE — GE Healthcare Finland OyTwitchView™ — BLINK DEVICE COMPANYHalyard — Avanos Medical, Inc.AVANOS — Avanos Medical, Inc.NMT cable — Shenzhen Mindray Bio-Medical Electronics Co., Ltd.Infinity Trident NMT SmartPod — DRAEGER MEDICAL SYSTEMS, INC.WiTOF — IDMEDTwitchView™ — BLINK DEVICE COMPANY
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2014-04-09 | GE Healthcare, LLC | When the E-NMT-01 module is used in conjunction with the ElectroSensor, the Neuromuscular Transmission (NMT) values may indicate a deeper level of muscle relaxa |
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