International safety notice
Diagnostické zdravotnické prostředky in vitro
Czech / Ksrzis · CZE · Jul 25, 2019
Key facts
| Title | Diagnostické zdravotnické prostředky in vitro |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | ONLINE TDM Vancomycin Gen.3 assay on cobas c platforms (VANC3) pro analyzátory cobas c311, cobas c501/502, cobas c 701/702, cobas c 503 |
| Manufacturer | Roche Diagnostics GmbH, Německo |
| Models | 21210, VANC3-APPLICATION, 08058849190, 06779336190, 4.0-80, GEN.3, KIN3”, SBN-CPS-2019-006, FSN-CPS-2019-006, 08445605190, 06779344190, VANC3 and 2 more |
| Event type | Safety Notice |
| Date | Jul 25, 2019 |
| 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