International safety notice
Technical name: Angiography Equipment
Brazil / Anvisa · BRA · Sep 22, 2017
Key facts
| Title | Technical name: Angiography Equipment |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Artis Angiography Equipment Technical name: Angiography Equipment ANVISA registration number: 10345162023 Risk class: III Affected model: Artis Q biplane; Affected serial numbers: 138042, 138125, 161013, 121125 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO SIEMENS HEALTHCARE DIAGNÓSTICOS SA CNPJ 01449930000190 AV MUTINGA 3800 4º ANDAR PIRITUBA SP FABRICANTE SIEMENS HEALTHCARE GMBH HENKESTRASSE127 91052 ERLANGEN ALEMANHA |
| Models | 138125, 138042, 10345162023, 121125, 161013 |
| Date | Sep 22, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 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