International safety notice
Electrodo de retorno MEGADYNE MEGA SOFT pediátrico Referencia 0840. UDI-DI 10614559103395
Spain / AEMPS · ESP · May 21, 2024
Key facts
| Title | Electrodo de retorno MEGADYNE MEGA SOFT pediátrico Referencia 0840. UDI-DI 10614559103395 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Electrodo de retorno MEGADYNE MEGA SOFT pediátrico Referencia 0840. UDI-DI 10614559103395 |
| Manufacturer | Megadyne Medical Products, Inc. Estados Unidos. |
| Models | ECHOSIGN_SIGNATUREBLOCK_0, 10614559103395, 2364349_ATTACHMENT, 136.226.215.26, 2024-05-21, 91.822.52.89, 106123, CBJCHBCAABAAKXDIUODYITE3XPUEUZRF4C-JPKVQ_P9W, 2024-253, 165.225.92.228, 28042, 28022 and 2 more |
| Event type | Safety Notice |
| Date | May 21, 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