International safety notice
Alert 2598 (Technovigilance) - Siemens Healthcare Diagnósticos Ltda - Artis Angiography Equipment - Possibility of sudden shutdown of the equipment due to a technical problem in the refrigeration unit.
Brazil / Anvisa · BRA · Jun 28, 2018
Key facts
| Title | Alert 2598 (Technovigilance) - Siemens Healthcare Diagnósticos Ltda - Artis Angiography Equipment - Possibility of sudden shutdown of the equipment due to a technical problem in the refrigeration unit. |
|---|---|
| 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 zee Affected serial numbers: 7230852L03, 7230852L08, 7230852L09 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO SIEMENS HEALTHCARE DIAGNÓSTICOS LTDA CNPJ 01449930000190 AV MUTINGA 3800 4º E 5º ANDAR PIRITUBA SÃO PAULO SP TEL 11 39082132 EMAIL FELIPEDEMELOFARIASIEMENSHEALTHINEERSCOM FABRICANTE DO PRODUTO SIEMENS HEALTHCARE GMBH SIEMENSSTR 1 91301 FORCHHEIM ALEMANHA |
| Models | 10345162023, 7230852L08, 7230852L03, 7230852L09 |
| Date | Jun 28, 2018 |
| 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