International safety notice
Neaktivní implantabilní zdravotnické prostředky
Czech / Ksrzis · CZE · Mar 16, 2018
Key facts
| Title | Neaktivní implantabilní zdravotnické prostředky |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | Capio™ SLIM Suture Capturing Device, Capio™ SLIM Suture Capturing Device (Box 5), Capio™ Open Access Suture Capturing Device (Box 4), Capio™ Standard Suture Capturing Device (Box 4), Capio™ RP Suture Capturing Device, Uphold™ LITE with Capio™ SLIM Vaginal Support System, Pinnacle™ Anterior Pelvic Floor Repair Kit, Pinnacle™ LITE Posterior with Capio SLIM Pelvic Floor Repair Kit |
| Manufacturer | Boston Scientific Corporation |
| Models | M0068318250, 53343, M0068318261, 95941, M0068311251, M0068318150, M0068321010, 78960, M0068312321, 00035, M0068318170, M0068317050 and 3 more |
| Event type | Safety Notice |
| Date | Mar 16, 2018 |
| 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