International safety notice
Sistema de endoprótesis cubierta periférica E-ventus BX
Spain / AEMPS · ESP · Mar 17, 2021
Key facts
| Title | Sistema de endoprótesis cubierta periférica E-ventus BX |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistema de endoprótesis cubierta periférica E-ventus BX |
| Manufacturer | JOTEC GmbH, Alemania. |
| Models | 28830, 7_09.09.2020, VI-2020-11, 2021-150, 11-09-2020, 26.100, 66532, 6487020, 2020-11, 91.822.52.89, 72379, BX_09.09.2020 and 1 more |
| Event type | Safety Notice |
| Date | Mar 17, 2021 |
At a glance
- No Recall
- Yes Field safety notice
- 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