International safety notice
Equipos Sonolith i-Sys (números de catálogo TMS 230793 / TMS 230795)
Spain / AEMPS · ESP · Feb 12, 2019
Key facts
| Title | Equipos Sonolith i-Sys (números de catálogo TMS 230793 / TMS 230795) |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Equipos Sonolith i-Sys (números de catálogo TMS 230793 / TMS 230795) |
| Manufacturer | EDAP TMS, Francia |
| Models | 69120, 902901514, 4.75.15.31.50, 28022, 4.72.15.31.51, 91.822.52.89, 230793, 2019-079, 230795, 46980, 49978 |
| Event type | Safety Notice |
| Date | Feb 12, 2019 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 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