International safety notice
Corrective action for the Digital Radiography X-Ray System DX-D 100 Type 5410 or DX-D 100 Wireless Type 5411, Agfa HealthCare NV
Germany / BfArM · DEU · Jun 22, 2015
Key facts
| Title | Corrective action for the Digital Radiography X-Ray System DX-D 100 Type 5410 or DX-D 100 Wireless Type 5411, Agfa HealthCare NV |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Digital Radiography X-Ray System DX-D 100 Type 5410 or DX-D 100 Wireless Type 5411, Agfa HealthCare NV |
| Manufacturer | Corrective action for the Digital Radiography X-Ray System DX-D 100 Type 5410 or DX-D 100 Wireless Type 5411, Agfa HealthCare NV |
| Models | DX-D100, PR1411200006, PR1406020002, PR1501190003, DR_DX_D_100, B-2640 |
| Date | Jun 22, 2015 |
| Regulator page | bfarm.de |
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