International safety notice
Technical name: Etest COLISTINA
Brazil / Anvisa · BRA · Jan 3, 2017
Key facts
| Title | Technical name: Etest COLISTINA |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: ETEST Colistina Technical name: Etest COLISTINA ANVISA registration number: 10158120623 Risk class: II Affected model: Affected serial numbers: Reference 537300: Lots 1004832200, 1004437930, 1004329220, 1004190730, 1004171220, 1003969990, 1003890030, 1003767080, 1003725600 1003610660, 1003532330, 1003514810, 1003409250, 1003297790, 002517610, 1002438560, 1002336190, 1002154530, 1001742150, 1001496200, 1001417080, 1001260560, 1001158900, 1000941970, 1000 893880, 1000756330, 1000714690. Reference 537308 : Lots 1004752310, 1004596710, 1004177660, 1003767090, 1003616140, 1003456440, 1003403320, 1002989530, 1002889130, 1002795210 , 1002703940, 1002523000, 1002343060, 1001744750, |
| Manufacturer | FABRICANTE BIOMERIEUX SA 3CHEMIN DU PORT MICHAUD 38390 LA BALME LES GROTTES |
| Models | 1003767090, 1002523000, 1004752310, 1001417080, 1003403320, 1004329220, 1002343060, 1001744750, 1003890030, 1002889130, 537308, 1003456440 and 37 more |
| Date | Jan 3, 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