International safety notice
Safety Notice for the device L-Varlock Instrument/ Implant box, KISCO International
Germany / BfArM · DEU · May 20, 2014
Key facts
| Title | Safety Notice for the device L-Varlock Instrument/ Implant box, KISCO International |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the device L-Varlock Instrument/ Implant box, KISCO International |
| Manufacturer | Safety Notice for the device L-Varlock Instrument/ Implant box, KISCO International |
| Models | 13532, 2.12‐1, BT0130, CAPA‐P‐2013‐039_FSCA, 12815 |
| Date | May 20, 2014 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No 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