International safety notice
Alert 2923 (Technosurveillance) Siemens Healthcare Artis Angiography Equipment Possibility that screws in the threaded union that connects the joint bearing to the ceiling support may become loose or break.
Brazil / Anvisa · BRA · Jul 12, 2019
Key facts
| Title | Alert 2923 (Technosurveillance) Siemens Healthcare Artis Angiography Equipment Possibility that screws in the threaded union that connects the joint bearing to the ceiling support may become loose or break. |
|---|---|
| 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 and Artiz Q; Affected serial numbers: 137099; |
| 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 | 137102, 164147, 147619, 109492, 164148, 10345162023, 103284, 137099 |
| Date | Jul 12, 2019 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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