International safety notice
Technical name: Misago Self-Expanding Peripheral Stent
Brazil / Anvisa · BRA · Aug 25, 2016
Key facts
| Title | Technical name: Misago Self-Expanding Peripheral Stent |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: Misago Self-Expanding Peripheral Stent ### Technical name: Misago Self-Expanding Peripheral Stent ### ANVISA registration number: 80012280143 ### Risk class: III (High Risk) ### Model(s) ) affected: ALL ### Batch(s): ANY AND ALL LOT MANUFACTURED FROM 2013 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO TERUMO MEDICAL DO BRASIL CNPJ 03129105000133 ENDEREÇO PRAÇA GENERAL GENTIL FALCÃO 108 9 ANDAR CJ 91 E 92 MUNICÍPIO SÃO PAULO UF SP TELEFONE DE CONTATO 11 35943845 FABRICANTE TERUMO COORPORATION ENDEREÇO 441 2CHOME HATAGAYA SHIBUYAKU TÓQUIO 1510072 JAPÃO |
| Models | 80012280143 |
| Date | Aug 25, 2016 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 1–9 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