International safety notice
Technical name: Identification Device; microorganism antibiogram
Brazil / Anvisa · BRA · Dec 22, 2017
Key facts
| Title | Technical name: Identification Device; microorganism antibiogram |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: E-test Family Technical name: Identification Device; microorganism antibiogram ANVISA registration number: 10158120623 Risk class: II Affected model: Teicoplanin. Affected serial numbers: 1005629730; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO BIOMERIEUX BRASIL IND E COM DE PROD LABORATORIAIS LTDA CNPJ 33040635000171 ESTRADA DO MAPUÁ 491 LOTE 1 TAQUARA RIO DE JANEIRO RJ FABRICANTE BIOMERIEUX SA 3 ROUTE DE PORT MICHAUD 38390 LA BALME LES GROTTES FRANÇA TELEFONE 33478877422 EMAIL SOPHIEDUCONGEREXTBIOMERIEUXCOM |
| Models | 1004989590, 1004107460, 1002312700, 1005629730, 1003454920, 1005201240, 1003108790, 1003759850, 1004637470, 1003104300, 1005201180, 1003956490 and 7 more |
| Date | Dec 22, 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