International safety notice
STENT
Brazil / Anvisa · BRA · Feb 13, 2012
Key facts
| Title | STENT |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | CORDIS EXPANDABLE STENT SYSTEM - registration 80145900749 - Lots: See attachment. http://portal.anvisa.gov.br/wps/wcm/connect/f008ce004a269a4ab06db9aa19e2217c/Alerta_1112_Lotes_afetados.pdf?MOD=AJPERES |
| Manufacturer | DETENTOR DO REGISTRO DO PRODUTO NO BRASIL JOHNSON JOHNSON DO BRASIL INDÚSTRIA E COMÉRCIO DE PRODUTOS PARA SAÚDE LTDA RUA GERIVATIBA Nº 207 12º AO 15º ANDARES SÃO PAULOSP |
| Models | 80145900749, Alerta_1112_Lotes_afetados.pdf?MOD=AJPERES, f008ce004a269a4ab06db9aa19e2217c |
| Date | Feb 13, 2012 |
| 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