International safety notice
Technical Name: Female Contraceptive Devices
Brazil / Anvisa · BRA · Jun 7, 2016
Key facts
| Title | Technical Name: Female Contraceptive Devices |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: ESSURE SYSTEM - Model: ESS305 - Registration No.: 80274190001 - Risk Class: IV ### UPDATE ON 11/29/2018: FROM 12/24/2018 THE TRANSFER OF OWNERSHIP OF THE PRODUCT REGISTRATION TO THE COMPANY BAYER S.A. - CNPJ 18.459.628/0001-15. |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO COMERCIAL COMMED PRODUTOS HOSPITALARES LTDA CNPJ 02643718000121 RUA BORGES LAGOA 1220 VILA CLEMENTINO CEP 04038001 SÃO PAULOSP FABRICANTE ESTRANGEIRO BAYER HEALTH CARE LLC 1011 MCCARTHY BLVD MILPITAS CALIFÓRNIA 95035 TELEFONE 1 862 404 5812 EMAIL DECLANMCGUINNESSBAYERCOM |
| Models | 80384380061, 18.459.628, ESS305, 0001-15, 80274190001 |
| Date | Jun 7, 2016 |
| 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