International safety notice
Valve for Hydrocephalus
Brazil / Anvisa · BRA · May 9, 2014
Key facts
| Title | Valve for Hydrocephalus |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Ventricular Catheter (AESCULAP HYDROCEPHALUS SYSTEM, Registration No. 80136990434 - batch: 4505252662 and PROGAV - GRAVITATIONAL VALVE FOR AESCULAP HYDROCEPHALY, Registration 80136990624 Series numbers/codes Annex) |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL LABORATÓRIOS B BRAUN SA CNPJ 31673254000102 ENDEREÇO AV EUGÊNIO BORGES 1092 E AV JEQUITIBÁ 9 SÃO GONÇALO RIO DE JANEIRO TELEFONE 21 26023263 |
| Models | 80136990624, 4505252662, 80136990434 |
| Date | May 9, 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