International safety notice
Diagnostické zdravotnické prostředky in vitro
Czech / Ksrzis · CZE · Apr 5, 2017
Key facts
| Title | Diagnostické zdravotnické prostředky in vitro |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | Instrument/Systems: cobas c 311 analyzer cobas c 501 module cobas c 502 module cobas c 701 module cobas c 702 module cobas 8000 ISE module 900 cobas 8000 ISE module 1800 with the specific accessories: PROBE SAMPLE, PROBE SAMPLE S, SAMPLE PROBE |
| Manufacturer | Hitachi High-Technologies Corporation (HHT) |
| Models | 0490235913, 0490252251, 0490256963, 0490257038, 0490233778, 0490233762, 04745914001, 0490237598, 0490252249, 24-BŘEZEN-2017, 16F9-10, 0490242330 and 211 more |
| Event type | Safety Notice |
| Date | Apr 5, 2017 |
| 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