International safety notice
TELIGEN 100 Double Chamber Implantable Cardioverter Defibrillator - Model: E110 - Registration: 10341350534 Risk Class IV
Brazil / Anvisa · BRA · Sep 23, 2014
Key facts
| Title | TELIGEN 100 Double Chamber Implantable Cardioverter Defibrillator - Model: E110 - Registration: 10341350534 Risk Class IV |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | TELIGEN 100 Double Chamber Implantable Cardioverter Defibrillator - Model: E110 - Registration: 10341350534 Risk Class IV - (AFFECTED SERIES ATTACHED) |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL BOSTON SCIENTIFIC DO BRASIL LTDA CNPJ 01513946000114 AV DAS NAÇÕES UNIDAS 21476 SANTO AMARO VILA ALMEIDA SÃO PAULOSP FONEFAX 11585325481158532663 EMAIL REGAFFAIRSBRAZILBSCICOM FABRICANTE BOSTON SCIENTIFIC CLONMEL LIMITED CASHEL ROADCLONMEL CO TIPPERARY IRLANDA |
| Models | 10341350534 |
| Date | Sep 23, 2014 |
| 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