International safety notice
General name: Probe for single-use laser guide Sales name: Medilus Light Guide
Japan / PMDA Recalls · JPN · Aug 14, 2025
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | General name: Probe for single-use laser guide Sales name: Medilus Light Guide |
| Manufacturer | Dornie Medtech Japan Co., Ltd. |
| Models | E-6100-BF, C5124S, K2310500 |
| Date | Aug 14, 2025 |
| Regulator page | info.pmda.go.jp |
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