International safety notice
Technical name: Ureterorenofibroscope
Brazil / Anvisa · BRA · Feb 15, 2017
Key facts
| Title | Technical name: Ureterorenofibroscope |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: Ureterorenofibroscope Technical name: Ureterorenofibroscope ANVISA registration number: 80124630193 Risk class: II Affected model: URF-P6/P6R Affected serial numbers: 2613119,2613237,2613239,2612933,2612936,2612947, 261H189, 2613101, 2612937, 2613240, 2613102,2613844,2613861,2613846,2613847,2613848,2613845,2613864,2613866. |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO OLYMPUS OPTICAL DO BRASIL LTDA ENDEREÇO RUA DO RÓCIO 430 2º ANDAR VILA OLIMPIA SP TELEFONE 30466400 RAMAL 6465 FABRICANTE OLYMPUS MEDICAL SYSTEMS CORP 2951 ISHIKAWACHO HACHIOJISHI TOQUIO JAPÃO EMAIL MARIKO1ARAIOTOLYMPUSCOJP |
| Models | 2613240, 2613846, 2613237, URF-P6, 2612937, 2613119, 2613102, 2613861, 80124630193, 2612933, 261H189, 2613864 and 9 more |
| Date | Feb 15, 2017 |
| 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