International safety notice
Linear Accelerator
Brazil / Anvisa · BRA · Dec 18, 2015
Key facts
| Title | Linear Accelerator |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | ARTISTE DIGITAL LINEAR CELERATOR - 10234230172 - Risk class III. |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL SIEMENS LTDA CNPJ 44013159000116 ENDEREÇO AV MUTINGA 3800 7º ANDAR PIRITUBA SÃO PAULO SP TELEFONE 0800 129 633 FABRICANTES SIEMENS AG HENKESTRASSE 127 ERLANGEN ALEMANHA SIEMENS MEDICAL SOLUTIONS USA INC 4040 NELSON AVENUE CONCORD CA ESTADOS UNIDOS |
| Models | 10514, 10321, 10234230172 |
| Date | Dec 18, 2015 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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