International safety notice
Updated Alert 2462 (Technovigilance) - Siemens Healthcare Diagnósticos S.A - Equipment for Angiography Potential fall of the upper compartment of the equipment table
Brazil / Anvisa · BRA · Jan 9, 2018
Key facts
| Title | Updated Alert 2462 (Technovigilance) - Siemens Healthcare Diagnósticos S.A - Equipment for Angiography Potential fall of the upper compartment of the equipment table |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Angiography Equipment Technical name: Angiography Equipment ANVISA registration number: 10234230075; Risk class: III Affected model: AXIOM Artis FC (Registration: 10234230075); Affected serial numbers: See attachment Updated list of serial numbers at risk |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO SIEMENS HEALTHCARE DIAGNÓSTICOS SA CNPJ 01449930000190 AV MUTINGA 3800 7º ANDAR PIRITUBA SÃO PAULO SP FABRICANTE SIEMENS AG SIEMENS HEALTHCARE GMBH SIEMENSTRASSE 1 DE91301 FORCHHEIM ALEMANHA |
| Models | 10234230093, 10345162023, 10234230075, 10234230096 |
| Date | Jan 9, 2018 |
| 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