International safety notice
Tubo endotraqueal de EMG NIM Trivantage. Modelos 8229706, 8229707, 8229708, 8229736, 8229737 y 8229738
Spain / AEMPS · ESP · Nov 27, 2023
Key facts
| Title | Tubo endotraqueal de EMG NIM Trivantage. Modelos 8229706, 8229707, 8229708, 8229736, 8229737 y 8229738 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Tubo endotraqueal de EMG NIM Trivantage. Modelos 8229706, 8229707, 8229708, 8229736, 8229737 y 8229738 |
| Manufacturer | Medtronic Xomed, Inc. Estados Unidos. |
| Models | 0225848738, 0226004326, 0225846916, 0226079291, 0226177688, 0226057749, 0226119539, 0226406353, 0226398929, 0226177689, 0226030095, 8229708 and 46 more |
| Event type | Safety Notice |
| Date | Nov 27, 2023 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers 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