International safety notice
PRODUCTO - Componente tibial del sistema de prótesis de rodilla Endo-Model – M - Componente tibial del sistema de prótesis de rodilla de rotación y bisagra Endo-Model SL Ver referencias en nota de aviso de la empresa.
Spain / AEMPS · ESP · Jun 7, 2024
Key facts
| Title | PRODUCTO - Componente tibial del sistema de prótesis de rodilla Endo-Model – M - Componente tibial del sistema de prótesis de rodilla de rotación y bisagra Endo-Model SL Ver referencias en nota de aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | PRODUCTO - Componente tibial del sistema de prótesis de rodilla Endo-Model – M - Componente tibial del sistema de prótesis de rodilla de rotación y bisagra Endo-Model SL Ver referencias en nota de aviso de la empresa. |
| Manufacturer | Waldemar Link GmbH & Co.KG, Alemania. |
| Models | 15-3818, 30.06.2024, 15-3815, 30.07.2024, 15-3816, 15-2834, 15-2838, DE2022, 80275, 15-2837, 17.06.2024, 91.822.52.89 and 25 more |
| Event type | Safety Notice |
| Date | Jun 7, 2024 |
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