International safety notice
Zdravotnické prostředky pro diagnostiku a terapii zářením
Czech / Ksrzis · CZE · Jan 28, 2019
Key facts
| Title | Zdravotnické prostředky pro diagnostiku a terapii zářením |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | Artis Q/Pheno systems (Systémy Artis Q / pheno a rentgenový generátor) |
| Manufacturer | Siemens Healthcare GmbH; Business Area Advanced Therapies, Německo |
| Models | 105024, 10848282, AX061, 10848353, AX060, 111102KAT, 20.2018, 121450, 2017\, 109483, 17.04, 109174 and 8 more |
| Event type | Safety Notice |
| Date | Jan 28, 2019 |
| Regulator page | eregpublicsecure.ksrzis.cz |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 Matching device models in FDA data
- 1–9 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