International safety notice
Neaktivní implantabilní zdravotnické prostředky
Czech / Ksrzis · CZE · Dec 22, 2017
Key facts
| Title | Neaktivní implantabilní zdravotnické prostředky |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | Cévní protézy Gelsoft™,Gelsoft™ ERS, Gelsoft™ Plus,Gelsoft™ Plus ERS, Gelseal™, Gelseal™ ERT, Gelweave™, K-Thin, K-Thin ERS, a Gelseal™ Plus, Cévní protézy Fluoropassiv™, Fluoropassiv™ ER, Thin Wall Fluoropassiv a Thin Wall Fluoropassiv ER, Kardiovaskulární látkové záplaty, Cévní protézy SealPTFE™ a Taperflo™ |
| Manufacturer | Vascutek Limited |
| Models | SR17-001, SP17-001, 7-001, FSNSP17001, 79773, FSNSP17-001 |
| Event type | Safety Notice |
| Date | Dec 22, 2017 |
| Regulator page | eregpublicsecure.ksrzis.cz |
At a glance
- No Recall
- Yes Field safety notice
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