International safety notice
Family of Products for Diagnostics for in vitro use, Imported
Brazil / Anvisa · BRA · Apr 24, 2014
Key facts
| Title | Family of Products for Diagnostics for in vitro use, Imported |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | COMMERCIAL NAME: Etest Family (ETEST ERTAPENEM) - Registration No. 10158120623 - Risk Class 2 (products of medium risk to the individual and/or low risk to public health, subject to registration) # LOTS: 2002110560; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO NO BRASIL BIOMÉRIEUX DO BRASIL SA ESTRADO DO MAPUÁ 491 TAQUARA JACAREPAGUÁ RIO DE JANEIRORJ FABRICANTE BIOMERIEUX LA BALME LED GROTTES 3 ROUTE DE PORT MICHAUD 38390 LA BALME LES GROTTES FRANÇA |
| Models | 2002110560, 1002389880, 1002054430, 10158120623 |
| Date | Apr 24, 2014 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers 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