International safety notice
MOSAIQ 1.0 y superior y Multi-ACCESS versiones 6.1 y superior que emplean: - Aceleradores lineales EXCI, TrueBeam y la consola Varian 4D con cuñas dinámicas mejoradas (EDW) o estáticas, - Aceleradores lineales de Siemens con cuñas virtuales (VW) o estátic
Spain / AEMPS · ESP · Dec 20, 2018
Key facts
| Title | MOSAIQ 1.0 y superior y Multi-ACCESS versiones 6.1 y superior que emplean: - Aceleradores lineales EXCI, TrueBeam y la consola Varian 4D con cuñas dinámicas mejoradas (EDW) o estáticas, - Aceleradores lineales de Siemens con cuñas virtuales (VW) o estátic |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | MOSAIQ 1.0 y superior y Multi-ACCESS versiones 6.1 y superior que emplean: - Aceleradores lineales EXCI, TrueBeam y la consola Varian 4D con cuñas dinámicas mejoradas (EDW) o estáticas, - Aceleradores lineales de Siemens con cuñas virtuales (VW) o estátic |
| Manufacturer | Elekta, Inc., Estados Unidos |
| Models | 91.822.52.89, 28034, 371-01-MSQ-013, 2018-661, 28022, 49374 |
| Event type | Safety Notice |
| Date | Dec 20, 2018 |
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