International safety notice
Technical name: Artis Angiography Equipment
Brazil / Anvisa · BRA · Sep 4, 2017
Key facts
| Title | Technical name: Artis Angiography Equipment |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Artis One Angiography Equipment Technical name: Artis Angiography Equipment ANVISA registration number: 10345162020 Risk class: III Affected model: N/A Affected serial numbers: 82200; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO SIEMENS HEALTHCARE DIAGNÓSTICOS SA CNPJ 01449930000190 AV MUTINGA 3800 7º ANDAR PIRITUBA SÃO PAULO SP FABRICANTE SIEMENS SHENZHEN MAGNETIC RESONANCE LTD SSMR SIEMENS MRI CENTER GAOXIN C AVE 2ND HITECH INDUSTRIAL PARK SHENZHEN GUANDONG CHINA |
| Models | 82046, 82067, 82143, 82032, 82161, 82062, 82030, 82170, 82084, 10345162020, 82187, 82200 and 8 more |
| Date | Sep 4, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 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