International safety notice
Technical name: Endoprosthesis (Vascular)
Brazil / Anvisa · BRA · Sep 18, 2017
Key facts
| Title | Technical name: Endoprosthesis (Vascular) |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Zenith Alpha Endovascular Graft Technical name: Endoprosthesis (Vascular) ANVISA registration number: 10212990315 Risk class: IV Affected model: ZTA-P-20-105 Numbers of series afetados: Lots: E3504880; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO E TAMUSSINO CIA LTDA CNPJ 33100082000103 RUA WASHINGTON LUIZ 97 E 95 LOJA B CENTRO RIO DE JANEIRO RJ FABRICANTE WILLIAM COOK EUROPE APS SANDET 6 DK4632 BJAEVERSKOV DINAMARCA EMAIL EUROPEANFIELDACTIONCOOKMEDICALCOM TELEFONE 353 61 334440 |
| Models | E3532655, E3504880, E3375482, E3313693, E3188739, E3375483, 10212990315, E3302173, E3387941, E3299689, ZTA-P-20-105 |
| Date | Sep 18, 2017 |
| 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