International safety notice
Neaktivní implantabilní zdravotnické prostředky
Czech / Ksrzis · CZE · Nov 10, 2017
Key facts
| Title | Neaktivní implantabilní zdravotnické prostředky |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | COLUMBUS REV FEMUR SPACER DISTAL F5, F6, F7, 15 mm; COLUMBUS REV FEMUR SPACER POST, F5, F6, F7, 15 mm |
| Manufacturer | Aesculap AG |
| Models | 65109852, 7461-95, VA02KA, NR486K, 51586632, 18532, 51447588, 726261, POST.F7, 51447596, CZ485, POST.F6 and 32 more |
| Event type | Safety Notice |
| Date | Nov 10, 2017 |
| 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