International safety notice
Sistemas de láser SuperPulsado SOLTIVE: - Pro SuperPulsed. Referencia: EGTFL-SLS, UDI-DI: 00821925044135. - Premium SuperPulsed. Referencia: EGTFL-PLS, UDI-DI: 00821925044111.
Spain / AEMPS · ESP · May 9, 2025
Key facts
| Title | Sistemas de láser SuperPulsado SOLTIVE: - Pro SuperPulsed. Referencia: EGTFL-SLS, UDI-DI: 00821925044135. - Premium SuperPulsed. Referencia: EGTFL-PLS, UDI-DI: 00821925044111. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistemas de láser SuperPulsado SOLTIVE: - Pro SuperPulsed. Referencia: EGTFL-SLS, UDI-DI: 00821925044135. - Premium SuperPulsed. Referencia: EGTFL-PLS, UDI-DI: 00821925044111. |
| Manufacturer | Gyrus ACMI, Inc. (Olympus Surgical Technologies America), EE UU |
| Models | 00821925044111, 00821925044135 |
| Event type | Safety Notice |
| Date | May 9, 2025 |
At a glance
- No Recall
- Yes 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