International safety notice
Commercial name: Echelon Reinforced - Micro Catheter - Registration No. 80301610021 - Risk Class: IV (Maximum Risk) - Technical Name: Catheters
Brazil / Anvisa · BRA · Jun 16, 2014
Key facts
| Title | Commercial name: Echelon Reinforced - Micro Catheter - Registration No. 80301610021 - Risk Class: IV (Maximum Risk) - Technical Name: Catheters |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Echelon Reinforced Micro Catheter - Registration 80301610021 - Risk Class IV ## Models: 105-5091-150; |
| Manufacturer | FABRICANTE MICRO THERAPEUTICS INC 9775 TOLEDO WAY CÓD POSTAL 92618 ESTADOS UNIDOS CALIFÓRNIA EMPRESA DETENTORA DO REGISTRO NO BRASIL EV3 COMÉRCIO DE PRODUTOS ENDOVASCULARES CNPJ 07072643000190 RESPONSÁVEL PELA AÇÃO DE CAMPO AUTO SUTURE DO BRASIL LTDA CNPJ 01645409000128 AVENIDA DAS NAÇÕES UNIDAS 12995 SÃO PAULOSP |
| Models | 80301610021, 105-5091-150, 5092-150, 105-5092-150, 145-5091-150, 190-5091-150 |
| Date | Jun 16, 2014 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 1–9 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