International safety notice
Technical name: Femoral component for knee arthroplasty
Brazil / Anvisa · BRA · Sep 14, 2017
Key facts
| Title | Technical name: Femoral component for knee arthroplasty |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: PL Femoral Component Technical name: Femoral component for knee arthroplasty ANVISA registration number: 80034760038 Risk class: III Affected model: 2630-506 Affected serial numbers: Registration: 80034760038 - model: 2630-506 Lot: 02331S - 10 units - Manufacturing Date: 03/31/2017. Registration: 80034760041 - model: 2630-306 Lot: 02539S - 10 units - Manufacturing Date: 04/18/2017. |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO META BIO INDUSTRIAL LTDA CNPJ 02513989000162 AVENIDA 37 N 1907 BAIRRO ESTÁDIO RIO CLARO SP FABRICANTE META BIO INDUSTRIAL LTDA AVENIDA 37 N 1907 BAIRRO ESTÁDIO RIO CLARO SP TELEFONE 019 35355303 EMAIL GERALDOZUMPANOVINCULACOMBR |
| Models | 2630-506, 80034760041, 02539S, 02331S, 2630-306, 80034760038 |
| Date | Sep 14, 2017 |
| 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