International safety notice
Technical name: Balloon catheter for peripheral angioplasty
Brazil / Anvisa · BRA · Oct 30, 2017
Key facts
| Title | Technical name: Balloon catheter for peripheral angioplasty |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Atlas Gold Dilation Catheter Technical name: Balloon catheter for peripheral angioplasty ANVISA registration number: 80689090119 Risk class: II Affected model: ATG120164 / ATG120202 / ATG120242 Affected serial numbers: 93NB0051 / 93NB0052 / 93YA0086 / 93YA0036 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO BARD BRASIL INDÚSTRIA E COMÉRCIO DE PRODUTOS MEDICOS LTDA CNPJ 10818693000188 RUA ALEXANDRE DUMAS 2100 10 ANDAR CHÁCARA SANTO ANTONIO SÃO PAULO SP FABRICANTE BARD PERIPHERAL VASCULAR INC 1625 WEST 3RD STREET TEMPE ARIZONA 85281 ESTADOS UNIDOS |
| Models | ATG120242, 80689090119, 93YA0036, 93NB0052, 93NB0051, ATG120202, 93YA0086, ATG120164 |
| Date | Oct 30, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 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