International safety notice
Angiography Equipment
Brazil / Anvisa · BRA · Mar 30, 2016
Key facts
| Title | Angiography Equipment |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | ARTIS ANGIOGRAPHY EQUIPMENT. |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL SIEMENS HEALTHCARE DIAGNÓSTICOS SA CNPJ 01449930000190 ENDEREÇO AV MUTINGA 3800 7º ANDAR PIRITUBA SÃO PAULOSP TELEFONE 0800 129 633 FABRICANTES SIEMENS AG WITTELSBACHERPLATZ 2 MÜNCHEN ALEMANHA SIEMENS HEALTHCARE GMBH HENKESTRASSE 127 ERLANGEN ALEMANHA SIEMENS AG SIEMENSTRASSE 1 FORCHHEIM ALEMANHA SIEMENS HEALTHCARE GMBH SIEMENSTRASSE 1 FORCHHEIM ALEMANHA |
| Models | 137020, 147650, 160843, 137088, 137160, 137411, 137161, 136918, 160457, 137182, 137143, 137246 and 58 more |
| Date | Mar 30, 2016 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 1–9 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