International safety notice
Technical name: Mobile X-ray Device
Brazil / Anvisa · BRA · Oct 6, 2017
Key facts
| Title | Technical name: Mobile X-ray Device |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: O´Arm 2 Mobile Imaging System Technical name: Mobile X-ray Device ANVISA registration number: 10339190638 Risk class: III Affected model: BI-700-02000 Affected serial numbers: C1389 C1320 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO MEDTRONIC COMERCIAL LTDA CNPJ 01772798000152 ENDEREÇO AV JORNALISTA ROBERTO MARINHO 85 10º ANDAR CEP 04675010 MUNICÍPIO SÃO PAULO SP E TELEFONE 11 21829200 FABRICANTE MEDTRONIC NAVIGATION INC ESTADOS UNIDOS DA AMÉRICA 300 FOSTER STREET LITTLETON MA 01460 |
| Models | C1320, 10339190638, BI-700-02000, C1389 |
| Date | Oct 6, 2017 |
| 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