International safety notice
Alert 2690 (Technosurveillance) - Olympus - Videobronchoscope - Bronchofibroscopio - Videorhinolaryngoscope - Ultrasound videoecobronchoscope - Possibility of loosening of the instrument channel door.
Brazil / Anvisa · BRA · Oct 3, 2018
Key facts
| Title | Alert 2690 (Technosurveillance) - Olympus - Videobronchoscope - Bronchofibroscopio - Videorhinolaryngoscope - Ultrasound videoecobronchoscope - Possibility of loosening of the instrument channel door. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial Name: Videobronchoscope / Bronchofibroscopio / Videorhinolaryngoscope / Ultrasound Videoecobronchoscope Technical Name: Flexible Endoscope ANVISA registration number: 80124630024/80124630018/80124630122/80124630128 Risk Class: II Modelo afetado: BF-160, BF-1T150, BF-1T180, BF-1T160, BF-1T240, BF-1T40, BF-1T60, BF-1TQ180, BF-3C160, BF-3C40, BF-40, BF-MP160F, BF-MP60, BF-P150, BF-P160, BF-P180, BF-P60, BF-Q180, BF-XP160F, BF-XP60, BF-XT160, BF-XT40, BF-UC180F, ENF-VT2. Affected serial numbers: All |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO OLYMPUS OPTICAL DO BRASIL LTDA CNPJ 04937243000101 RUA DO RÓCIO 430 2º ANDAR VILA OLIMPIA SÃO PAULO SP TEL 30466400 RAMAL 6465 EMAIL QUALIDADEBRASILOLYMPUSCOM FABRICANTE DO PRODUTO OLYMPUS MEDICAL SYSTEMS CORP 2951 ISHIKAWA CHO HACHIOJISHI TÓQUIO JAPÃO |
| Models | BF-XP160F, BF-1T180, BF-P150, BF-1T150, BF-1T60, ENF-VT2, BF-P180, BF-XT160, BF-1T160, BF-1T240, BF-3C40, BF-P60 and 16 more |
| Date | Oct 3, 2018 |
| 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