International safety notice
Electrodos de retorno reutilizables para paciente MEGADYNE MEGA SOFT y MEGA 2000. Ver códigos de productos y UDI-DI afectados en la nota de aviso de la empresa.
Spain / AEMPS · ESP · Jun 30, 2023
Key facts
| Title | Electrodos de retorno reutilizables para paciente MEGADYNE MEGA SOFT y MEGA 2000. Ver códigos de productos y UDI-DI afectados en la nota de aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Electrodos de retorno reutilizables para paciente MEGADYNE MEGA SOFT y MEGA 2000. Ver códigos de productos y UDI-DI afectados en la nota de aviso de la empresa. |
| Manufacturer | Megadyne Medical Products, Inc., EE.UU. |
| Models | 10614559101797, MROSAFI1, 91.822.52.89, 10614559100936, 2015.006.30527, 10614559101872, 22851, 28022, 2268964, 28042, 2023-305, 248275-230515 and 12 more |
| Event type | Safety Notice |
| Date | Jun 30, 2023 |
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