International safety notice
Technical name: Ultrasound device
Brazil / Anvisa · BRA · Jul 28, 2017
Key facts
| Title | Technical name: Ultrasound device |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Ultrasound Diagnostic System Technical name: Ultrasound device ANVISA registration number: 10295030071 Risk class: II Affected model: TUS-X100; Number of series files: W5D1693377; N5D1692777; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO TOSHIBA MEDICAL DO BRASIL LTDA CNPJ 46563938000110 AVENIDA CECI 328 TAMBORÉ BARUERI SP FABRICANTE TOSHIBA MEDICAL SYSTEMS CORPORATION 1385 SHIMOISHIGAMI OTAWARASHITOCHIGI3248550JAPÃO |
| Models | W5B1722542, N5D1692769, W5B1732963, BRB1732003, AEA1732019, TUS-AI800, AEA1732023, N5D1692772, N5D1692771, W5D1693381, AEA1732021, TUS-X200 and 59 more |
| Date | Jul 28, 2017 |
| 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