International safety notice
Elekta Oncentra Brachy - rekonstrueerimisviga ning tegeliku ja planeeritud doosijaotuse erinevus
Estonia / EMDDB · EST · Nov 1, 2022
Key facts
| Title | Elekta Oncentra Brachy - rekonstrueerimisviga ning tegeliku ja planeeritud doosijaotuse erinevus |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Elekta Oncentra Brachy |
| Manufacturer | ELEKTA ONCENTRA BRACHY |
| Models | 08717213052307, 08717213053700, 08717213051782, 08717213051843, 08717213052321, 08717213053717, 806-01-BTP-003, 08717213051294, 08717213052239, 08717213052314, 08717213051775, 08717213052291 and 5 more |
| Date | Nov 1, 2022 |
| Regulator page | terviseamet.ee |
At a glance
- No Recall
- No Field safety notice
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