International safety notice
Catéter de dilatación periférico Passeo-35 Xeo y Sistema de stent periférico expandible por balón Dynetic-35
Spain / AEMPS · ESP · Jan 26, 2022
Key facts
| Title | Catéter de dilatación periférico Passeo-35 Xeo y Sistema de stent periférico expandible por balón Dynetic-35 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Catéter de dilatación periférico Passeo-35 Xeo y Sistema de stent periférico expandible por balón Dynetic-35 |
| Manufacturer | Biotronik AG, Suiza |
| Models | 428873, 428864, 08213996, 08213348, 428863, 428887, 448944, 428909, 08215721, 428738, 09210274, 08214901 and 52 more |
| Event type | Safety Notice |
| Date | Jan 26, 2022 |
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