International safety notice
CareLink SmartSync Base & Patient connector (Zařízení SmartSync Device Manager podporující kardiostimulátory Azure™ a kardiostimulátory pro srdeční resynchronizační terapii Percepta™, Serena™, Solara™)
Czech / Ksrzis · CZE · Jun 12, 2020
Key facts
| Regulator | Czech / Ksrzis |
|---|---|
| Country | CZE |
| Brand | CareLink SmartSync Base & Patient connector (Zařízení SmartSync Device Manager podporující kardiostimulátory Azure™ a kardiostimulátory pro srdeční resynchronizační terapii Percepta™, Serena™, Solara™) |
| Manufacturer | Medtronic Inc., USA |
| Models | 64583562, 3.2.01, FA917, 24970A, CZ2427000000000081880264, 00CZECH, 41171, CZ699005618, 81880264, 24967 |
| Event type | Safety Notice |
| Date | Jun 12, 2020 |
| 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