International safety notice
Alert 2979 (Technovigilance) - Siemens Healthcare Diagnósticos LTDA - Angiography Equipment Possibility of liquids entering critical locations.
Brazil / Anvisa · BRA · Aug 27, 2019
Key facts
| Title | Alert 2979 (Technovigilance) - Siemens Healthcare Diagnósticos LTDA - Angiography Equipment Possibility of liquids entering critical locations. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial Name: Artis Angiography Equipment (registration 10345161980); Technical Name: Angiography Equipment ANVISA registration number: 10345161980; Risk Class: III Affected model: Artis zee ceiling (registration 10345161980); 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 7º ANDAR PIRITUBA SÃO PAULO SP TEL 11 39082132 EMAIL FELIPEDEMELOFARIASIEMENSHEALTHINEERSCOM FABRICANTE DO PRODUTO SIEMENS AG ALEMANHA REGISTROS 10345161980 10234230096 10234230075 10345162005 SIEMENS HEALTHCARE GMBH ALEMANHA REGISTROS 10345162023 E 10345162005 |
| Models | 10345161980, 10345162005, 10234230075, 10345162023, 10234230096 |
| Date | Aug 27, 2019 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
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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