International safety notice
Zdravotnické prostředky pro diagnostiku a terapii zářením
Czech / Ksrzis · CZE · Apr 23, 2019
Key facts
| Title | Zdravotnické prostředky pro diagnostiku a terapii zářením |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | Prestige II, Prestige VH, Prestige SI (GE Medical Systems SCS, Francie) Flexmed, Prestilix 1600X (GE CGR, Belgie) PROTEUS XR/A, SILHOUETTE VR (GE Hualun Medical Systems Co.Ltd, Čína) Precision 500D (GE Medical, Systems LLC, USA) |
| Manufacturer | GE CGR, Belgie GE Medical Systems SCS, Francie GE Hualun Medical Systems Co.Ltd, Čína GE Medical, Systems LLC, USA |
| Models | 819523PRESTIGE, B5111113, 4813MPH, SA1050RX05, M5505607, M2718125, M4265604, 615791W2, B5346201, D4185521, B5174303, M9409524 and 813 more |
| Event type | Safety Notice |
| Date | Apr 23, 2019 |
| Regulator page | eregpublicsecure.ksrzis.cz |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 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