International safety notice
Ecógrafos bk3500, bk3000, bk5000 y bkActiv 2300, con opción de batería.
Spain / AEMPS · ESP · Sep 30, 2024
Key facts
| Title | Ecógrafos bk3500, bk3000, bk5000 y bkActiv 2300, con opción de batería. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Ecógrafos bk3500, bk3000, bk5000 y bkActiv 2300, con opción de batería. |
| Manufacturer | BK Medical Aps, Dinamarca. |
| Models | 91.822.52.89, BK3500, 05704916000264, 08174, BK3000, 87012, 2024-523, 28022, BK5000, RECALL.FMI87012, 111237 |
| Event type | Safety Notice |
| Date | Sep 30, 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