International safety notice
Technical name: BALLOON CATHETER FOR PERIPHERAL ANGIOPLASTY
Brazil / Anvisa · BRA · Aug 30, 2016
Key facts
| Title | Technical name: BALLOON CATHETER FOR PERIPHERAL ANGIOPLASTY |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: POWERCROSS DILATION CATHETER 0.018 OTW PTA Technical name: BALLOON CATHETER FOR PERIPHERAL ANGIOPLASTY ANVISA registration number: 10349000474 Risk class: II Affected model: AB18W030200150 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO AUTO SUTURE DO BRASIL LTDA ENDEREÇO AV JORNALISTA ROBERTO MARINHO 85 10º ANDAR CEP 04675010 UF SP MUNICÍPIO SÃO PAULO TELEFONE 11 21829200 FABRICANTE NOME EV3 INC ENDEREÇO4600 NATHAN LANE NORTH PLYMOUTH MN 55442 EUA |
| Models | AB18W030200150, 10349000474 |
| Date | Aug 30, 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