International safety notice
Technical Name: Stent for peripheral arteries
Brazil / Anvisa · BRA · Jun 14, 2016
Key facts
| Title | Technical Name: Stent for peripheral arteries |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial Name: NITINOL CORDIS STENTS (Stent for peripheral arteries), Registration 80145901077. Risk classification IV-Maximum Risk. |
| Manufacturer | O DETENTOR DE REGISTRO DO STENTS DE NITINOL CORDIS É A EMPRESA JOHNSON JOHNSON DO BRASIL IND E COM DE PROD PARA SAÚDE LTDA CNPJ 54516661000101 LOCALIZADA NA RUA GERIVATIVA N 207 SÃO PAULO SP CONTATOS FONE 12 39327977 EMAIL GBUOSIITSJNJCOM QUE O FABRICANTE DOS PRODUTOS AFETADOS É A EMPRESA CORDIS CORPORATION LOCALIZADA NOS ESTADOS UNIDOS DA AMÉRICA |
| Models | 80145901077 |
| Date | Jun 14, 2016 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1,000+ Matching device models in FDA data
- 100–999 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