International safety notice
CATHETERS
Brazil / Anvisa · BRA · Sep 6, 2011
Key facts
| Title | CATHETERS |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | MULTI LUMENS CENTRAL VENOUS CATHETER - Registered with Anvisa under number 10216830011 - Model DUPLO LUMEN 4FR X 13cm - Lot RF 0087800. |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL GABMED PRODUTOS ESPECÍFICOS LTDA RUA ANTONIO DAS CHAGAS 966 CHÁCARA SANTO ANTONIO SÃO PAULOSP |
| Models | 10216830011, 0087800 |
| Date | Sep 6, 2011 |
| 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