International safety notice
Technical name: LINEAR ACCELERATOR
Brazil / Anvisa · BRA · Aug 26, 2016
Key facts
| Title | Technical name: LINEAR ACCELERATOR |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: ARTISTE DIGITAL LINEAR ACCELERATOR ### Technical name: LINEAR ACCELERATOR ### ANVISA registration number: 10234230172 ### Risk class: III (High Risk) ### Affected model: Artiste ### Affected serial numbers: 10233; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO SIEMENS HEALTHCARE DIAGNÓSTICOS SA CNPJ 01449930000190 ENDEREÇO AV MUTINGA 3800 7º ANDAR PIRITUBA SÃO PAULOSP TELEFONE 0800 129 633 FABRICANTES SIEMENS MEDICAL SOLUTIONS USA INC 685 EAST MIDDLEFIELD ROAD MOUNTAIN VIEW CALIFORNIA 94043 ESTADOS UNIDOS SIEMENS AG HENKESTRASSE 127 DE95478 KEMNATH |
| Models | 10234230172, 10321, 10233 |
| Date | Aug 26, 2016 |
| 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