International safety notice
Neaktivní implantabilní zdravotnické prostředky
Czech / Ksrzis · CZE · Jan 25, 2018
Key facts
| Title | Neaktivní implantabilní zdravotnické prostředky |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | 2M insert 15° for MUTARS® RS cup and LUMiC® TiN |
| Manufacturer | implantcast GmbH |
| Models | 23.02.2018, 13485, 02424448, 02423839, 21614, 17002, FSCA_17002, 744-0, VOOT.6D, NOLADE21HAM, 02424652, 120629 and 4 more |
| Event type | Safety Notice |
| Date | Jan 25, 2018 |
| 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