International safety notice
MAGNETOM Magnetic Resonance Equipment
Brazil / Anvisa · BRA · Nov 24, 2014
Key facts
| Title | MAGNETOM Magnetic Resonance Equipment |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Magnetic resonance equipment, SIEMENS brand, Risk class II, of the following models: - Magnetom Aera/ Magnetom Skya, Registro: 10234230175 /// - Magnetom Avanto, Registration:10234230095 /// - Magnetom Espree, Registro: 10234230115 /// - Magnetom Essence and Verio, Register:10234230155 /// - Magnetom Harmony, Registration: 10234230056 (risk class III) /// - Magnetom Sonata, Registro: 10234230089 /// - Magnetom Spectra, Registry: 10234230182 /// - Magnetom Symphony, Registro: 10234230057 /// - Magnetom Trio, Registro: 10234230098 /// Serial numbers: attached. |
| Manufacturer | DETENTORA DO REGISTRO NO BRASIL SIEMENS LTDA CNPJ 44013159000116 ENDEREÇO AV MUTINGA 3800 7º ANDAR PIRITUBA SÃO PAULO SP FABRICANTE SIEMENS AG MEDICAL SOLUTIONS GROUP ENDEREÇO HENKESTRASSE 127 DE91052 ERLANGEN ALEMANHA |
| Models | 10234230056, 10234230095, 10234230098, 10234230175, 10234230182, 10234230089, 10234230155, 10234230115, 10234230057 |
| Date | Nov 24, 2014 |
| 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.
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