International safety notice
Urgent Field Safety Notice for FiLaC Fistula Kit, LHP® Procedure Kit, HeLP Procedure Kit by CeramOptec GmbH, a company of biolitec group
Germany / BfArM · DEU · Apr 30, 2021
Key facts
| Title | Urgent Field Safety Notice for FiLaC Fistula Kit, LHP® Procedure Kit, HeLP Procedure Kit by CeramOptec GmbH, a company of biolitec group |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | FiLaC Fistula Kit, LHP® Procedure Kit, HeLP Procedure Kit |
| Manufacturer | CeramOptec GmbH, a company of biolitec group |
| Models | 910101, A.4086.1, 19E0081, FSN-2021-04-12, 19F0271, A.40238, 9796799, D-53121, 96799, 482536, 18G01, 482534 and 7 more |
| Date | Apr 30, 2021 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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