International safety notice
Aktivní implantabilní zdravotnické prostředky
Czech / Ksrzis · CZE · Oct 11, 2019
Key facts
| Title | Aktivní implantabilní zdravotnické prostředky |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | Adapta Versa Sensia Relia Attesta Sphera Vit. AEGQ (kardiostimulátor) |
| Manufacturer | Medtronic Inc. |
| Models | REVDD01, ATDRL1, E50A1, VSF20, CZ2427000000000081880264, Q80A2, FA857, ADDRL1, VEDR01, SPDRL1, REDR01, G70A2 and 31 more |
| Event type | Safety Notice |
| Date | Oct 11, 2019 |
| Regulator page | eregpublicsecure.ksrzis.cz |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 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