International safety notice
Technical Name: VIDEODUODENOSCOPES (Flexible Endoscopes)
Brazil / Anvisa · BRA · Mar 9, 2016
Key facts
| Title | Technical Name: VIDEODUODENOSCOPES (Flexible Endoscopes) |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial Name: Videoduodenoscopes // Anvisa Registration Number: 10371280029 // Risk Class: II Medium Risk // Affected Model: ED-3490TK // Affected Serial Number: H110761, H110763 and H110765 |
| Manufacturer | DADOS DO DETENTOR DO REGISTRO NO BRASIL ETENTOR DO REGISTRO NA ANVISA PENTAX MEDICAL BRASIL MATERIAIS E EQUIPAMENTOS LTDA AV POMPÉIA 1792 2O ANDAR CJ 07 VILA POMPÉIA SÃO PAULO SP CEP 05022001 CNPJ 01716863000101 FONE 11 36753935 OU 28927469 EMAIL EDUARDOMIRANDAPENTAXMEDICALCOM OU VANIANERYPENTAXMEDICALCOM FABRICANTE HOYA CORPORATION PENTAX MIYAGI FACTORY 302 OKADA AZASHIMOMIYANO TUSKIDATE KURIHARASHI MIYAGI JAPÃO |
| Models | ED-3490TK, H110763, H110765, 10371280029, H110761 |
| Date | Mar 9, 2016 |
| 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