International safety notice
Technical name: Device for Microorganism Identification/Antibiogram
Brazil / Anvisa · BRA · Jan 26, 2018
Key facts
| Title | Technical name: Device for Microorganism Identification/Antibiogram |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: - BD Phoenix Gram Negative; Technical name: Device for Microorganism Identification/Antibiogram ANVISA registration number: 10033430636; Risk class: II Affected model: BD Phoenix NMIC 203; Affected serial numbers: PX2049; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO BECTON DICKINSON INDÚSTRIAS CIRÚRGICAS LTDA CNPJ 21551379000106 AVENIDA PRESIDENTE JUSCELINO KUBITSCHEK 273 JUIZ DE FORA MG FABRICANTE BECTON DICKINSON AND COMPANY 7 LOVETON CIRCLE SPARKS MARYLAND 21152 ESTADOS UNIDOS EMAIL CRISTINAMALMEIDABDCOM TELEFONE 11 5185 9810 |
| Models | PX2049, PX2134, 10033430734, PX2079, PX2078, PX2098, PX2063, PX2099, PX2120, PX2121, 10033430636, PX2097 |
| Date | Jan 26, 2018 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
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