International safety notice
Technical name: Systema VITEK MS
Brazil / Anvisa · BRA · Mar 2, 2017
Key facts
| Title | Technical name: Systema VITEK MS |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: VITEK MS Technical name: Systema VITEK MS ANVISA registration number: 10158120668 Risk class: I Affected model: Vitek MS V2.0 and Vitek MS V 3.0 - Clinic |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO BIOMÉRIEUX BRASIL INDÚSTRIA E COMÉRCIO DE PRODUTOS LABORATORIAIS LTDA CNPJ 33040635000171 ENDEREÇO ESTR MAPUÁ 491 LOTE 1 TAQUARA RIO DE JANEIRO RJ TELEFONE EMAIL DE CONTATO 08000264848 CONTATOBIOMERIEUXCOM FABRICANTE BIOMÉRIEUX SA ENDEREÇO F 69280 MARCY LETOILE FRANÇA |
| Models | 10158120668 |
| Date | Mar 2, 2017 |
| 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