International safety notice
Alert 2638 (Technosurveillance) - Siemens Healthcare - Equip.
Brazil / Anvisa · BRA · Aug 8, 2018
Key facts
| Title | Alert 2638 (Technosurveillance) - Siemens Healthcare - Equip. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade Name: Artis Angiography Equipment / Angiography Equipment / Axiom Artis FA / Axiom Artis FC Technical Name: Angiography Equipment ANVISA registration number: 10345162023 / 10234230096/ 10234230093 / 10234230075 Risk Class: III Modelo afetado: Artis Q biplane / Artis Q ceiling / Artis Q floor / Artis zee biplane / Artis zee ceiling / Artis zee floor / Artis zeego / AXIOM Artis dFA / AXIOM Artis dFC / AXIOM Artis FA / AXIOM Artis FC Affected serial numbers: See attachment List of serial numbers at risk |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO SIEMENS HEALTHCARE DIAGNÓSTICOS LTDA CNPJ 01449930000190 AV MUTINGA 3800 4º E 5º ANDAR PIRITUBA SÃO PAULO SP TEL 11 39081649 EMAIL JAQUELINESANTOSSIEMENSHEALTHINEERSCOM FABRICANTE DO PRODUTO SIEMENS HEALTHCARE GMBH SIEMENSSTR 1 91301 FORCHHEIM ALEMANHA |
| Models | 10234230096, 10234230093, 10345162023, 10234230075 |
| Date | Aug 8, 2018 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
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