International safety notice
Aplicación de programador del médico Activa para estimulación profunda. Modelo A610.
Spain / AEMPS · ESP · Apr 23, 2019
Key facts
| Title | Aplicación de programador del médico Activa para estimulación profunda. Modelo A610. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Aplicación de programador del médico Activa para estimulación profunda. Modelo A610. |
| Manufacturer | Medtronic Inc., EEUU. |
| Models | 30C, 37612, 37601, SOFTWARE1.0.3470, 51478, CT900, 1.0.3470, 91.822.52.89, FA861, 37603, 37602, 28022 and 3 more |
| Event type | Safety Notice |
| Date | Apr 23, 2019 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models 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