International safety notice
Angiography Equipment
Brazil / Anvisa · BRA · Oct 2, 2015
Key facts
| Title | Angiography Equipment |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | AXIOM ARTIS, Artis dFA and Artis dFC models, registration 10234230096; |
| Manufacturer | DETENTORA DO REGISTRO NO BRASIL SIEMENS LTDA CNPJ 44013159000116 ENDEREÇO AV MUTINGA 3800 7º ANDAR PIRITUBA SÃO PAULO SP FABRICANTE SIEMENS AG ENDEREÇO WITTELSBACHERPLATZ 2 DE80333 MUENCHEN ALEMANHA |
| Models | 35862, 35885, 35318, 35485, 35913, 35817, 35751, 35884, 50138, 35622, 10234230096, 35729 and 8 more |
| Date | Oct 2, 2015 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 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