International safety notice
Angiography Equipment
Brazil / Anvisa · BRA · Aug 26, 2015
Key facts
| Title | Angiography Equipment |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | ARTIS ANGIOGRAPHY EQUIPMENT, Registration 10234230190 - Serial Numbers: 121125 |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL SIEMENS LTDA CNPJ 44013159000116 ENDEREÇO AV MUTINGA 3800 7º ANDAR PIRITUBA SÃO PAULO SÃO PAULO TELEFONE 11 39083876 FABRICANTE SIEMENS AG WITTELSBACHERPLATZ 2 DE80333 MUENCHEN ALEMANHA |
| Models | 121125, 10234230190 |
| Date | Aug 26, 2015 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 100–999 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