International safety notice
CATHETERS
Brazil / Anvisa · BRA · Aug 15, 2011
Key facts
| Title | CATHETERS |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | LOGICATH CENTRAL VENOUS CATHETER FOR HEMODIALYSIS - DOUBLE LUMEN - Registration 80228990022 and LOGICATH CENTRAL VENOUS CATHETER FOR HEMODIALYSIS - TRIPLE LUMEN - Registration 80228990019 - CODES AND LOTS as per attached list. |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL SMITHS MEDICAL DO BRASIL PRODUTOS HOSPITALARES LTDA AVENIDA PAULISTA 1048 1º ANDAR CJ 11 CENTRO SÃO PAULOSP |
| Models | 80228990019, 80228990022, 5vfyz |
| Date | Aug 15, 2011 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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