International safety notice
DEVICE FOR IDENTIFICATION/ANTIBIOGRAM OF MICROORGANISMS
Brazil / Anvisa · BRA · Jul 24, 2015
Key facts
| Title | DEVICE FOR IDENTIFICATION/ANTIBIOGRAM OF MICROORGANISMS |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | ETEST FAMILY - CEFOTAXIME 100TIRAS, REGISTRATION 10158120623, RISK CLASS II, LOT 1002377890 (VALIDITY 06/06/2015) |
| Manufacturer | DETENTOR DO REGISTRO BIOMERIEUX BRASIL SA CNPJ 33040635000171 ENDEREÇO ESTRADA MAPUÁ 491 RIO DE JANEIRO FABRICANTE BIOMERIEUX SA ENDEREÇO 3 CHEMIN DU PORT MICHAUD 383900 LA BALME LES GROTTES FRANÇA |
| Models | 10158120623, 1002377890, 100TIRAS |
| Date | Jul 24, 2015 |
| 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