International safety notice
Magnetic Resonance Equipment
Brazil / Anvisa · BRA · Dec 23, 2015
Key facts
| Title | Magnetic Resonance Equipment |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Magnetom MRI device, model Open, Impact and Vision, registration 10234230012, series: 7449; |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL SIEMENS HEALTHCARE DIAGNÓSTICOS SA CNPJ 01449930000190 ENDEREÇO AV MUTINGA 3800 7º ANDAR PIRITUBA SÃO PAULOSP TELEFONE 0800 129 633 FABRICANTES SIEMENS AG WITTELSBACHERPLATZ 2 MÜNCHEN ALEMANHA SIEMENS SHENZHEN MAGNETIC RESONANCE LTD SIEMENS MRI CENTER GAOXIN C AVENUE 2ND HITECH INDUSTRIAL PARK SHENZHEN GUANGDONG 518057 CHINA SIEMENS HEALTHCARE DIAGNÓSTICOS SA RUA DONA FRANCISCA 8300 BLOCO K MÓDULO 1 JOINVILLESC BRASIL |
| Models | 53501, 10345162004, 73003, 10234230203, 21120, 42031, 10234230057, 10234230155, 22202, 71365, 71338, 22388 and 56 more |
| Date | Dec 23, 2015 |
| 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