International safety notice
Alert 2220 (Technosurveillance) Siemens ARTISTE / ONCOR / PRIMUS LINEAR DIGITAL ACCELERATOR Display of incorrect values
Brazil / Anvisa · BRA · Feb 24, 2017
Key facts
| Title | Alert 2220 (Technosurveillance) Siemens ARTISTE / ONCOR / PRIMUS LINEAR DIGITAL ACCELERATOR Display of incorrect values |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: ARTISTE DIGITAL LINEAR ACCELERATOR / ONCOR / PRIMUS Technical name: Linear Accelerator ANVISA registration number: 10234230125/10234230172/10234230073 Risk class: III Affected model: MD4 Acetabulum Affected serial numbers (updated): 3221; Access the full content of Alert 2220 with the respective annexes on the ANVISA Portal (http://portal.anvisa.gov.br/alertas). |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO SIEMENS HEALTHCARE DIAGNÓSTICOS SA CNPJ 01449930000190 ENDEREÇO AV MUTINGA 3800 7º ANDAR PIRITUBA SÃO PAULOSP TELEFONE 0800 129 633 FABRICANTE SIEMENS AG HENKESTRASSE 127 DE91052 ERLANGEN ALEMANHA SIEMENS MEDICAL SOLUTIONS USA INC 4040 NELSON AVENUE 94520 CONCORD CALIFORNIA ESTADOS UNIDOS |
| Models | 10234230073, 70-4118, 70-4203, 10234230125, 10234230172, 70-5062, 70-4246 |
| Date | Feb 24, 2017 |
| 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