International safety notice
Sistema Kodak DirectView DR 3000 y Sistema Kodak DirectView DR 3500
Spain / AEMPS · ESP · Jan 30, 2020
Key facts
| Title | Sistema Kodak DirectView DR 3000 y Sistema Kodak DirectView DR 3500 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistema Kodak DirectView DR 3000 y Sistema Kodak DirectView DR 3500 |
| Manufacturer | Carestream Health Inc., Estados Unidos |
| Models | MA-2019-004, 57398, 30001015, 91.822.52.89, 28224, 28022, 35000060, SERIE35000030, 3000SISTEMA, 2020-056, 35000030 |
| Event type | Safety Notice |
| Date | Jan 30, 2020 |
At a glance
- No Recall
- Yes 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