International safety notice
Neaktivní implantabilní zdravotnické prostředky
Czech / Ksrzis · CZE · Apr 25, 2019
Key facts
| Title | Neaktivní implantabilní zdravotnické prostředky |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | Integra Movement Great Toe Systém (Náhrada metatarzofalangeálního kloubu) |
| Manufacturer | Integra LifeSciences (Ascension Orthopedics), USA |
| Models | SZ.30, MGT-890-40MT, T-890-10MT, MGT-890-20MT, MGT-89020MT, 11101, INTEGRA0, MGT-890-10MT, MGT-890-10MT—, SZ.10, MGT-890-30MT, POU2IVAJIJAKO and 14 more |
| Event type | Safety Notice |
| Date | Apr 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