International safety notice
Diagnostické zdravotnické prostředky in vitro
Czech / Ksrzis · CZE · Jul 20, 2017
Key facts
| Title | Diagnostické zdravotnické prostředky in vitro |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | VITEK® 2 GN ID, VITEK® 2 GP ID, VITEK® 2 YST ID, VITEK® 2 BCL ID, VITEK® 2 NH ID, VITEK® 2 ANC ID, VITEK® 2 AST |
| Manufacturer | bioMérieux Inc |
| Models | 5400238243, 1320264103, 2410000203, 6140171203, 413724, 2760186403, 1010209203, 2750210203, 412604, 2850209403, 413401, 414164 and 663 more |
| Event type | Safety Notice |
| Date | Jul 20, 2017 |
| 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