International safety notice
Technical name: Magnetic Resonance Equipment
Brazil / Anvisa · BRA · Oct 31, 2016
Key facts
| Title | Technical name: Magnetic Resonance Equipment |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: Magnetic Resonance Equipment Technical name: Magnetic Resonance Equipment ANVISA registration number: 10345162032 Risk class: II Affected model: MAGNETOM AERA, MAGNETOM SKYRA Affected serial numbers: 12811009 ; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO SIEMENS HEALTHCARE DIAGNÓSTICOS SA CNPJ 01449930000190 ENDEREÇO AV MUTINGA 3800 7º ANDAR PIRITUBA SÃO PAULOSP TELEFONE 0800 129 633 FABRICANTE SIEMENS HEALTHCARE GMBH HENKESTRASSE 127 91052 ERLANGEN ALEMANHA SIEMENS HEALTHCARE DIAGNÓSTICOS SA RUA DONA FRANCISCA 8300 BLOCO K MODULO 1 PARTE 1 89219600 JOINVILLE SC BRASIL SIEMENS SHENZHEN MAGNETIC RESONANCE LTD SIEMENS MRI CENTER GAOXIN C AVE 2ND HITECH INDUSTRIAL PARK SHENZHEN GUANGDONG 518057 CHINA |
| Models | 12811009, 128110100, 10345162032 |
| Date | Oct 31, 2016 |
| 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