International safety notice
IMPLANT FOR ANEURYSM
Brazil / Anvisa · BRA · Jan 17, 2013
Key facts
| Title | IMPLANT FOR ANEURYSM |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | PIPELINE EMBOLIZATION DEVICE - Registration 80301610006 - AFFECTED MODELS/LOTS: SEE ANNEX. http://portal.anvisa.gov.br/wps/wcm/connect/f4094c804e37c340a02cb3c09d49251b/Lote_Afetados_no_Brasil.pdf?MOD=AJPERES |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL EV3 COMÉRCIO DE PRODUTOS ENDOVASCULARES DO BRASIL LTDA SÃO PAULOSP |
| Models | f4094c804e37c340a02cb3c09d49251b, 80301610006 |
| Date | Jan 17, 2013 |
| 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