International safety notice
femoral cable
Brazil / Anvisa · BRA · Jun 22, 2016
Key facts
| Title | femoral cable |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Femoral Drill Handle ANVISA registration number: 80005430069 Risk class: I Affected model(s): CODE 09309003 All batches manufactured between January 1995 and October 2005. |
| Manufacturer | DETENTOR DO REGISTRO DO PRODUTO NO BRASIL STRYKER DO BRASIL LTDA CNPJ 02966317000102 ENDEREÇO RUA URUSSUÍ 300 7 ANDAR MUNICÍPIO SÃO PAULO UF SP TELEFONE DE CONTATO 11 51892503 FABRICANTE STRYKER ORTHOPAEDICS ENDEREÇO RAHEEN BUSINESS PARK RAHEEN CO LIMERICK IRLANDA |
| Models | 09309003, 80005430069 |
| Date | Jun 22, 2016 |
| 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