International safety notice
in vitro diagnostic kit
Brazil / Anvisa · BRA · Jan 7, 2014
Key facts
| Title | in vitro diagnostic kit |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | ZYM B / API NH / API LISTERIA - Anvisa Registration nº 10158120560/ 10158120563/10158120563, respectively |
| Manufacturer | BIOMERIEUX SA FRANÇA |
| Models | 10158120563, 10158120560 |
| Date | Jan 7, 2014 |
| 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