International safety notice
Zdravotnické prostředky pro diagnostiku a terapii zářením
Czech / Ksrzis · CZE · Sep 27, 2019
Key facts
| Title | Zdravotnické prostředky pro diagnostiku a terapii zářením |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | FDR GO (Mobilní rtg systém FUJIFILM FDR Go) |
| Manufacturer | SHIMADZU Corporation, Japonsko |
| Models | 2019．6．28, 81-75-823, 800KAT, MQ0001283008, MQ000128A007, MQ000128A021, MQ0001283012, SQBR19024, MQ0001289034, MQ0001281007, MQ0001289035, MQ0001281030 and 82 more |
| Event type | Safety Notice |
| Date | Sep 27, 2019 |
| Regulator page | eregpublicsecure.ksrzis.cz |
At a glance
- No Recall
- Yes 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