International safety notice
BritePro / BriteBlade Single Use Fibre Optic
Czech / Ksrzis · CZE · Nov 19, 2019
Key facts
| Regulator | Czech / Ksrzis |
|---|---|
| Country | CZE |
| Brand | BritePro / BriteBlade Single Use Fibre Optic |
| Manufacturer | Flexicare Medical Limited, Velká Británie |
| Models | 180900401, 040-342, QA079, 181102912, 15.11.2019, 040-333, 040-713, 181100301, 2019-001 |
| Event type | Safety Notice |
| Date | Nov 19, 2019 |
| 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