International safety notice
CARDIOVASCULAR PROSTHESIS
Brazil / Anvisa · BRA · Sep 6, 2010
Key facts
| Title | CARDIOVASCULAR PROSTHESIS |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | CORE VALVE REVALVING SYSTEM - Registered with Anvisa under number 80065320080 - Affected batches - 14AUG2009J - 22AUG2009K - 07DEC2009E - 08FEB2010I - 23APR2010E - See also the distribution list. (http://portal.anvisa.gov.br/wps/wcm/connect/4684eb8043dbffd5bdd4bf4eca73f154/alerta+1028+2010+lista+distribui%C3%A7%C3%A3o+.pdf?MOD=AJPERES) |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL CMS PRODUTOS HOSPITALARES LTDA RUA 53 216 JARDIM GOIAS CEP 74810210 GOIÂNIA GOIÁS FONEFAX 6240080800 |
| Models | 07DEC2009E, 08FEB2010I, 22AUG2009K, 4684eb8043dbffd5bdd4bf4eca73f154, 23APR2010E, 14AUG2009J, 80065320080 |
| Date | Sep 6, 2010 |
| 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