International safety notice
Commercial name: Elecsys Estradiol II Assay (Registration No.: 10287410228) and Elecsys Estradiol III Assay (Registration No.: 10287411088)///Product code: 3000079190 and 6656021190./// Product risk class: Class II.
Brazil / Anvisa · BRA · Apr 1, 2016
Key facts
| Regulator | Brazil / Anvisa |
|---|---|
| Country | BRA |
| Brand | Commercial name: Elecsys Estradiol II Assay (Registration No.: 10287410228) and Elecsys Estradiol III Assay (Registration No.: 10287411088)///Product code: 3000079190 and 6656021190./// Product risk class: Class II. |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO ROCHE DIAGNÓSTICA BRASIL LTDA CNPJ 30280358000186 ENDEREÇO AVENIDA ENGENHEIRO BILLINGS 1729 PRÉDIO 38 SÃO PAULO SP BRASILTECNOVIGILANCIAROCHECOM EMPRESA FABRICANTE ROCHE DIAGNOSTICS GMBH ENDEREÇO SANDHOFER STRASSE 116 68305 ALEMANHA |
| Models | 6656021190, 10287411088, 3000079190, 10287410228 |
| Date | Apr 1, 2016 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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