International safety notice
Urgent Field Safety Notice for Laryngeal Electrodes, Urethral Electrodes, Disposable needle electrodes for EEG and EMG, Disposable Stimulation Probes by SPES Medica Srl
Germany / BfArM · DEU · May 17, 2021
Key facts
| Title | Urgent Field Safety Notice for Laryngeal Electrodes, Urethral Electrodes, Disposable needle electrodes for EEG and EMG, Disposable Stimulation Probes by SPES Medica Srl |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | EEG and EMG, Disposable Stimulation Probes |
| Manufacturer | SPES Medica Srl |
| Models | MN20G3342I, MN20G3135I, MNCSC625DST, UR20F2699I, UE002, LSE3463DCA200, MN20G3171I, MN4013D101, MN20G3504I, MN20F2990I, LS20G3360I, D039045401 and 29 more |
| Date | May 17, 2021 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1