International safety notice
Linear Accelerator
Brazil / Anvisa · BRA · May 25, 2015
Key facts
| Title | Linear Accelerator |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Affected equipment: ONCOR linear accelerator, model: Oncor Impression Plus, risk class III, registration: 10234230125, affected series: 5529 /// Artiste digital linear accelerator, risk class III, registration 10234230172, affected series: 5867. |
| Manufacturer | DETENTORA DO REGISTRO NO BRASIL SIEMENS LTDA CNPJ 44013159000116 ENDEREÇO AV MUTINGA 3800 7º ANDAR PIRITUBA SÃO PAULO SP FABRICANTE SIEMENS MEDICAL SOLUTIONS INC E SIEMENS AG ENDEREÇO 4040 NELSON AVENUE CONCORD CA 94520 ESTADOS UNIDOS E ROENTGENSTRASSE 1921 D95478 KEMNATH |
| Models | 10234230172, 10234230125 |
| Date | May 25, 2015 |
| Regulator page | anvisa.gov.br |
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