International safety notice
Single incident during the use of a flexible implant tube with blind end from Varian
Germany / BfArM · DEU · Oct 19, 2005
Key facts
| Title | Single incident during the use of a flexible implant tube with blind end from Varian |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Single incident during the use of a flexible implant tube with blind end from Varian |
| Manufacturer | Single incident during the use of a flexible implant tube with blind end from Varian |
| Models | CH-6303, 2724-2836, 01333-000, 44-1293-601219, 1293-601-327, 20063, 7313-0, 78535, 30067, 732-381-5300, 770-955-1775, 42781 and 47 more |
| Date | Oct 19, 2005 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 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