International safety notice
Technical Name: System for total multicompartmental femoro-tibio-patellar arthroplasty Risk Class: III - HIGH RISK
Brazil / Anvisa · BRA · Jun 3, 2013
Key facts
| Title | Technical Name: System for total multicompartmental femoro-tibio-patellar arthroplasty Risk Class: III - HIGH RISK |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: PROSTHESIS FOR KNEE ARTHROPLASTY Risk Class: III - HIGH RISK Registration Number: 10171110029 Registration Validity: 12/22/2014 |
| Manufacturer | BIOMECÂNICA INDÚSTRIA E COMÉRCIO DE PRODUTOS ORTOPÉDICOS LTDA BRASIL CNPJ 58526047000173 |
| Models | 10171110029 |
| Date | Jun 3, 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