International safety notice
Aktivní implantabilní zdravotnické prostředky
Czech / Ksrzis · CZE · Jan 7, 2019
Key facts
| Title | Aktivní implantabilní zdravotnické prostředky |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | S-ICD system's SQ-RH Model 1010 Pulse Generator (Jednokomorový implantabilní defibrilátor) |
| Manufacturer | Cardiac Pacemaker Inc., USA |
| Models | 0.006, 90-DAY, 709-22, VÝKONU2, 3MĚSÍČNÍM, CHECKS1, EXPECTATIONS2, 90DENNÍ, 1010–, 1675-1681, 3-MONTH, 92297476-FA |
| Event type | Safety Notice |
| Date | Jan 7, 2019 |
| 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