International safety notice
Technical name: VITEK AST N 239 Card
Brazil / Anvisa · BRA · May 24, 2017
Key facts
| Title | Technical name: VITEK AST N 239 Card |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: VITEK AST N 239 Card - Colistina (cs01n) Technical name: VITEK AST N 239 Card ANVISA registration number: 10158120592 Risk class: II Affected model: not applicable |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO BIOMÉRIEUX BRASIL IND COM DE PROD LAB LTDA CNPJ 33040635000171 ESTR MAPUÁ 491 LOTE 1 TAQUARA RIO DE JANEIRO RJ TEL 21 0800 026 4848 FABRICANTE BIOMÉRIEUX INC 595 ANGLUM ROAD HAZELWOOD MO 63042 USA ST LOUIS |
| Models | 10158120592, cs01n |
| Date | May 24, 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