International safety notice
Technical Name: Catheter with Infusion Port
Brazil / Anvisa · BRA · Jan 13, 2014
Key facts
| Title | Technical Name: Catheter with Infusion Port |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | BARDPORT FULLY IMPLANTABLE IN PLASTIC AND SILICONE - Registration: 10178010192 - Risk Class: IV - MAXIMUM RISK |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL POLITEC IMPORTAÇÃO E COMÉRCIO LTDA CNPJ 43894609000164 ENDEREÇO ALAMEDA ARAGUACEMA Nº 138 BAIRRO TAMBORÉ BARUERISP FABRICANTE BARD ACCESS SYSTEMS ESTADOS UNIDOS 605 NORTH 5600 WEST SALT LAKE CITY UTAH |
| Models | 10178010192 |
| Date | Jan 13, 2014 |
| 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