International safety notice
Diagnostické zdravotnické prostředky in vitro
Czech / Ksrzis · CZE · Jan 19, 2018
Key facts
| Title | Diagnostické zdravotnické prostředky in vitro |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | OptiView DAB IHC Detection Kit, ultraView Universal DAB Detection Kit, ultraView Universal DAB Detection Kit, ultraView SISH Detection Kit, CINtec PLUS Cytology Kit (CE-IVD), OptiView Amplification Kit, OptiView Amplification Kit (250 Test), ultraView SISH DNP Detection Kit, Hematoxylin II |
| Manufacturer | Ventana Medical Systems Inc |
| Models | Y15384, Y22162, 06889549001, Y19322, 06718663001, Y22153, Y11687, Y15133, Y09284, Y11834, Y17984, Y15435 and 39 more |
| Event type | Safety Notice |
| Date | Jan 19, 2018 |
| Regulator page | eregpublicsecure.ksrzis.cz |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models 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