International safety notice
Aplicación del programador del médico para DBS (Estimulación Cerebral Profunda) modelo A610
Spain / AEMPS · ESP · Oct 4, 2021
Key facts
| Title | Aplicación del programador del médico para DBS (Estimulación Cerebral Profunda) modelo A610 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Aplicación del programador del médico para DBS (Estimulación Cerebral Profunda) modelo A610 |
| Manufacturer | Medtronic Inc. EE.UU. |
| Models | 28022, 72589, 0X4B81F1A3, 0X791EBFE0, SOFTWARE3.0.1048, 2.0.4594, V.2.0.X, 3.0.1062, 28050, P-5-2, 3.0.1048, FA1188 and 8 more |
| Event type | Safety Notice |
| Date | Oct 4, 2021 |
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