International safety notice
Extended corrective actions for Kodak 2100 and Kodak 2200 Intraoral X-ray systems, Carestream Health
Germany / BfArM · DEU · Feb 17, 2014
Key facts
| Title | Extended corrective actions for Kodak 2100 and Kodak 2200 Intraoral X-ray systems, Carestream Health |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Kodak 2100 and Kodak 2200 Intraoral X-ray systems, Carestream Health |
| Manufacturer | Extended corrective actions for Kodak 2100 and Kodak 2200 Intraoral X-ray systems, Carestream Health |
| Models | 14608, MA-2013-0037 |
| Date | Feb 17, 2014 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 10–99 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