International safety notice
STENT INTRACRANIANO
Brazil / Anvisa · BRA · Feb 22, 2012
Key facts
| Title | STENT INTRACRANIANO |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | STENT WINGSPAN - Registro 80005430258 - Ref.90741728-FA - NÚMEROS DOS PRODUTOS: M003WE0250090; M003WE0250150; M003WE0250200; M003WE0300090; M003WE0300150; M003WE0300200; M003WE0350090; M003WE0350150; M003WE0350200; M003WE0400090; M003WE0400150; M003WE0400200; M003WE0450090; M003WE0450150; M003WE0450200 - TODOS OS LOTES. |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL STRYKER DO BRASIL LTDA RUA AMÉRICO BRASILIENSE Nº 1000 SÃO PAULOSP FONE 01151892517 |
| Models | M003WE0400150, M003WE0400090, M003WE0300150, M003WE0250200, Ref.90741728-FA, M003WE0350150, M003WE0350090, M003WE0350200, 80005430258, M003WE0250090, M003WE0300090, M003WE0250150 and 5 more |
| Date | Feb 22, 2012 |
| 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