International safety notice
Implantable Defibrillator.
Brazil / Anvisa · BRA · Dec 20, 2011
Key facts
| Title | Implantable Defibrillator. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | TELIGEN 100 IMPLANTABLE CARDIOVERR DEFIBRILLATOR, Model E102 (Anvisa registration no. 10341350535); |
| Manufacturer | DETENTOR DE REGISTRO NO BRASIL BOSTON SCIENTIFIC DO BRASIL LTDA CNPJ 01513946000114 END AVENIDA MARIA COELHO AGUIAR 215 BLOCO F 6 ANDAR CEP 05804900 SÃO PAULOSP TEL 11 58532244 FAX 11 58532663 CONTATO ELIANE VILELA ASSUNTOS REGULATÓRIOS VILELAEBSCICOM TEL 11 58532522 |
| Models | 10341350535, 10341350534, 10341350536 |
| Date | Dec 20, 2011 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1,000+ Matching device models in FDA data
- 1,000+ 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