International safety notice
Electrodos de retorno reutilizables para paciente: - MEGADYNE MEGA SOFT: Referencias 0830 y 0835. - MEGADYNE MEGA 2000: Referencias 0800. Ver UDI-DI en la nota de aviso de la empresa.
Spain / AEMPS · ESP · Jun 26, 2024
Key facts
| Title | Electrodos de retorno reutilizables para paciente: - MEGADYNE MEGA SOFT: Referencias 0830 y 0835. - MEGADYNE MEGA 2000: Referencias 0800. Ver UDI-DI en la nota de aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Electrodos de retorno reutilizables para paciente: - MEGADYNE MEGA SOFT: Referencias 0830 y 0835. - MEGADYNE MEGA 2000: Referencias 0800. Ver UDI-DI en la nota de aviso de la empresa. |
| Manufacturer | Megadyne Medical Products, Inc; EE UU. |
| Models | 10614559101872, 10614559100936, 28022, 165.225.92.223, 0835.MEGADYNE, 2024-337, 2024-06-24, 2000™, ECHOSIGN_SIGNATUREBLOCK_0, 10614559101797, 91.822.52.89, 2024_ES-ES and 6 more |
| Event type | Safety Notice |
| Date | Jun 26, 2024 |
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