International safety notice
Diagnostické zdravotnické prostředky in vitro
Czech / Ksrzis · CZE · Feb 4, 2019
Key facts
| Title | Diagnostické zdravotnické prostředky in vitro |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | VITEK® 2 Identification (ID) / Antimicrobial Susceptibility Test (AST) Cards |
| Manufacturer | bioMerieux Inc., USA |
| Models | 7950805203, 27‐FEB‐20, AST-XN06, AST-XN01, 417952, 2750809103, 23-AUG-19, 415670, AST-N261, 5410812203, 25-FEB-20, AST-N379 and 169 more |
| Event type | Safety Notice |
| Date | Feb 4, 2019 |
| Regulator page | eregpublicsecure.ksrzis.cz |
At a glance
- No Recall
- Yes Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 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