International safety notice
catheter
Brazil / Anvisa · BRA · Nov 3, 2015
Key facts
| Title | catheter |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | SOUNDSTAR ECO CATHETER and EP NAVIGATION SYSTEM - CARTO 3 System, Model Catheters and Surgical Navigation System. |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL JOHNSON JOHNSON DO BRASIL IND E COM DE PROD PARA SAÚDE LTDA CNPJ 54516661000101 ENDEREÇO RUA GERIVATIBA NO 207 SÃO PAULO SÃO PAULO TELEFONE 12 3932 1659 FABRICANTE BIOSENSE WEBSTER INC PORTO RICO |
| Models | 51018, 51021, 51022, 80145901453, 51020, 50530, 11879, 50573, 50572, 50532, 50128, 50203 and 2 more |
| Date | Nov 3, 2015 |
| 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