International safety notice
Technical name: Angiography Equipment
Brazil / Anvisa · BRA · Mar 6, 2017
Key facts
| Title | Technical name: Angiography Equipment |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: ARTIS ANGIOGRAPHY EQUIPMENT Technical name: Angiography Equipment ANVISA registration number: 80015490090 Risk class: III Affected model: Artis Zee Ceiling,, Artis Zee Floor, Artis Zee biplane, Artis Zeego, Artis Q biplane |
| 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 WITTELSBACHERPLATZ 2 DE80333 MUENCHEN ALEMANHA |
| Models | 80015490090 |
| Date | Mar 6, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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