International safety notice
Diagnostické zdravotnické prostředky in vitro
Czech / Ksrzis · CZE · Nov 9, 2018
Key facts
| Title | Diagnostické zdravotnické prostředky in vitro |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | Accu-Chek® Inform II system, CoaguChek Pro II system, CoaguChek® XS Plus system, CoaguChek® XS Pro system, cobas h 232 POC system, cobas h 232 POC system |
| Manufacturer | Roche Diagnostics GmbH, Německo |
| Models | 03.01.2006, 04.00.04, AUG-2018, 04.03.2000, 04901126190, 05530199160, 05060303001, 07210841190, 04805658160, 04901142018, 04800842190, 14000 and 23 more |
| Event type | Safety Notice |
| Date | Nov 9, 2018 |
| 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