International safety notice
Device for identification/antibiogram of microorganisms
Brazil / Anvisa · BRA · Sep 14, 2016
Key facts
| Title | Device for identification/antibiogram of microorganisms |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: BD Phoenix Gram Negative /// Technical name: Device for identification / antibiogram of microorganisms /// ANVISA registration number: 10033430636 /// Risk class: II /// Considering that cefepime is present in BD Phoenix panels Gram Negatives, the Customer Notification included all panels that are already used, that is, panels already registered with ANVISA, and potential panels to be used, that is, panels that are about to be registered. |
| Manufacturer | FABRICANTE BECTON DICKINSON AND COMPANY 7 LOVETON CIRCLE SPARKS MD 21152 EUA DETENTOR DO REGISTRO BECTON DICKINSON INDÚSTRIAS CIRÚRGICAS LTDA CNPJ 21551379000106 AV PRESIDENTE JUSCELINO KUBITSCHEK 273 JUIZ DE FORA MG |
| Models | ID-407, ID-406, NMIC-406, UNMIC-407, 10033430636 |
| Date | Sep 14, 2016 |
| 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