International safety notice
Technical Name: Catheters
Brazil / Anvisa · BRA · Mar 30, 2016
Key facts
| Title | Technical Name: Catheters |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: ARROW INTRA-AORTIC BALLOON CATHETER (IAB) - FIBEROPTIX ## ANVISA registration number: 80004970002## Risk class: III ## Affected model(s): IAB-05830-LWS/ IAB-05840- LWS ## Affected Models/Lot(s): IAB-05840-LWS/LOT: 18F14H0060 - IAB-05830-LWS/LOT: 18F14H003 |
| Manufacturer | DADOS DO DETENTOR DO REGISTRO NO BRASIL ISOMEDICAL COMERCIAL CNPJ 00757668000188 ENDEREÇO R GUILHOBEL 41 VILA MONTE ALEGRE SÃO PAULOSP DADOS DO FABRICANTE ARROW INTERNATIONAL INC 9 PLYMOUTH STREET EVERETTMA 02149 |
| Models | IAB-05840-LWS, IAB-05830-LWS, 18F14H003, 80004970002, 18F14H0060 |
| Date | Mar 30, 2016 |
| 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