International safety notice
Diagnostické zdravotnické prostředky in vitro
Czech / Ksrzis · CZE · Nov 30, 2017
Key facts
| Title | Diagnostické zdravotnické prostředky in vitro |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | Screening panel 123, Cellbind P2, Cellbind P3, Column screen 123 |
| Manufacturer | Sanquin Reagents B.V. |
| Models | K3005, 8000242941, 72108000XXXXXXREAGENTS, 26-10-201, 82452042, 8000242937, 67177565, 8---242937, 23032017, K5010LOT, 8---242941, K7230 and 37 more |
| Event type | Safety Notice |
| Date | Nov 30, 2017 |
| Regulator page | eregpublicsecure.ksrzis.cz |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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