International safety notice
Tubos endotraqueales de EMG reforzado estándar NIM™ y NIM CONTACT™. Ver números de modelo y UDI de los productos afectados en la nota de aviso de la empresa.
Spain / AEMPS · ESP · Feb 23, 2024
Key facts
| Title | Tubos endotraqueales de EMG reforzado estándar NIM™ y NIM CONTACT™. Ver números de modelo y UDI de los productos afectados en la nota de aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Tubos endotraqueales de EMG reforzado estándar NIM™ y NIM CONTACT™. Ver números de modelo y UDI de los productos afectados en la nota de aviso de la empresa. |
| Manufacturer | Medtronic Xomed, Inc. EEUU. |
| Models | 33832575, 00763000745837, 00763000745868, 0064316978957900763000745868, 2023-11, 8229306, 8229508, 00763000882396, 0064316978956200763000745851, 00643169789524, 00643169358713, 79699 and 28 more |
| Event type | Safety Notice |
| Date | Feb 23, 2024 |
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