International safety notice
Urgent Field Safety Notice for ARTIFLEX phakic IOL, ARTIFLEX toric phakic IOL by Ophtec BV
Germany / BfArM · DEU · Oct 6, 2021
Key facts
| Title | Urgent Field Safety Notice for ARTIFLEX phakic IOL, ARTIFLEX toric phakic IOL by Ophtec BV |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | ARTIFLEX phakic IOL, ARTIFLEX toric phakic IOL |
| Manufacturer | Ophtec BV |
| Models | 8717819ARTIFLEX401, 206001W, 15-09-2021, 8717819ARTISAN206, 8717819ARTISAN203, 204001W, 8717819ARTISANTORIC, 203001W, C21-009, 40114SW, L23-HV0209.PDF, L23-HV5310.PDF and 3 more |
| Date | Oct 6, 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