International safety notice
Ultrasound device
Brazil / Anvisa · BRA · Apr 19, 2016
Key facts
| Title | Ultrasound device |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name of the product: EPIQ Diagnostic Ultrasound Equipment/// Registration number: 10216710275/// affected model: EPIQ 7/// Product risk class: II. |
| Manufacturer | DETENTOR DO REGISTRO PHILIPS MEDICAL SYSTEMS LTDA CNPJ 58295213000178 ENDEREÇO AV TAMBORÉ 14001440 BOX 31 A 33 TAMBORÉ BARUERISP BRASIL CEP 06460000 TELEFONE PARA SUPORTE 08007017789 FABRICANTE PHILIPS ULTRASOUND INC ENDEREÇO 22100 BOTHELL EVERETT HIGHWAY BOTHELL WA 980218431 EUA |
| Models | 10216710275 |
| Date | Apr 19, 2016 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 Matching catalog numbers 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