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Catalogue (356)
Page 8 of 8| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Neuro Omega LeadConfirm P Adaptor | Neuro Omega LeadConfirm P Adaptor | FDA UDI | Class II | Active |
| NeuroNav Headstage cable | Headstage cable | FDA UDI | Class II | Active |
| Bengun Adapter | Bengun Adapter | FDA UDI | Class II | Active |
| Remote control NN | Remote control NN | FDA UDI | Class II | Active |
| Power cable | Plug Type G | FDA UDI | Class II | Active |
| Alphatemp Clinical Thermometer | K813333 | FDA 510(k) | Class II | Active |
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Sep 4, 2018 | Z-1216-2019 | — | terminated | If cables are improperly connected, current may reach high charge density, causing tissue harm. |