International safety notice
Stent Cardiovascular
Brazil / Anvisa · BRA · Dec 2, 2015
Key facts
| Title | Stent Cardiovascular |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Affected products: (1). |
| Manufacturer | DETENTOR DO REGISTRO ABBOTT LABORATÓRIOS DO BRASIL LTDA CNPJ 56998701000116 ENDEREÇO RUA MICHIGAN 735 BROOOKLIN SÃO PAULO SP FABRICANTE REGISTRO80146501896 ABBOTT CARDIOVASCULAR ENDEREÇO 3200 LAKESIDE DRIVE SANTA CLARA CA 95054 ESTADOS UNIDOS REGISTRO 80146501969 CASHEL ROAD CLONMEL CO TIPPERARY IRLANDA |
| Models | 1012464-12, 1012464-18, 1234300-28, 1012462-28, 1234250-28, 1012463-23, 1012462-08, 1012464-23, 80146501896, 1012462-12, 1234250-08, 1234300-18 and 18 more |
| Date | Dec 2, 2015 |
| 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