International safety notice
Diagnostické zdravotnické prostředky in vitro
Czech / Ksrzis · CZE · Aug 14, 2019
Key facts
| Title | Diagnostické zdravotnické prostředky in vitro |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | Makropanel 16, Makropanel 16P K1148 - Screening panel K5010 - Column Screen 123 K7210 - Cellbind P3 K7211 - Cellbind P3-P |
| Manufacturer | Sanquin Reagents B.V. |
| Models | 72108000249041, 8000249042, 9190AMSTERDAM, 8000249041, 2018-08-02, 12896, 13252795, 8000249038, 8000249033, 5123570, ET6SEN, K1384 and 48 more |
| Event type | Safety Notice |
| Date | Aug 14, 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