International safety notice
Neaktivní implantabilní zdravotnické prostředky
Czech / Ksrzis · CZE · Nov 11, 2020
Key facts
| Title | Neaktivní implantabilní zdravotnické prostředky |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | InterStim Percutaneous Extension |
| Manufacturer | Medtronic Inc., USA |
| Models | 978B1, CZ699005618, 81880264, 978A1, 3560022, 3560030, 00CZECH, 64583562, FA933, CZ2427000000000081880264, FA21-04, 41171 |
| Event type | Safety Notice |
| Date | Nov 11, 2020 |
| Regulator page | eregpublicsecure.ksrzis.cz |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models 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