International safety notice
Tubo endotraqueal de EMG reforzado estándar NIM™ y Tubo endotraqueal de EMG reforzado NIM CONTACT™
Spain / AEMPS · ESP · May 20, 2022
Key facts
| Title | Tubo endotraqueal de EMG reforzado estándar NIM™ y Tubo endotraqueal de EMG reforzado NIM CONTACT™ |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Tubo endotraqueal de EMG reforzado estándar NIM™ y Tubo endotraqueal de EMG reforzado NIM CONTACT™ |
| Manufacturer | Medtronic Xomed, Inc. EEUU. |
| Models | M726750C793, 8229506, 8229306, 916250400, 28050, FA1255, 8229308, 28022, 8229307, 8229508, 2022-241, 91.822.52.89 and 3 more |
| Event type | Safety Notice |
| Date | May 20, 2022 |
At a glance
- No Recall
- Yes Field safety notice
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