ANVISA registration
Instrumental Joelho - Revisão Tíbia/Fêmur (SCORE® Revisão) - Versão Mecânica/Navegada
Registration 80726260022. Kit Instrumental
Registration details
| Registration number | 80726260022 |
|---|---|
| Application number | 25351693686201439 |
| Technical name | Kit Instrumental |
| Risk class | I |
| Published on | 22/12/2014 |
| Validity | Indefinite validity |
Registration holder
| Legal name | AMPLITUDE LATIN AMERICA S.A. |
|---|---|
| CNPJ | 10.978.692/0001-09 |
Manufacturer
- AMPLITUDE SAS FRANÇA
Other registrations held by AMPLITUDE LATIN AMERICA S.A.view all
INSTRUMENTAL PARA APLICAÇÕES DO JOELHO UNICOMPARTIMENTAL SCORE AMPLITUDE
80726260008Instrumental Joelho - Corte Patelar (SCORE® Primário) Versão Mecânica
80726260011Instrumental Quadril - Prótese Femoral Revisão (GENERIC / INTEGRALE)
80726260014Instrumental Quadril - Fresa Acetabular - Versão Mecânica
80726260015Instrumental Joelho - Tíbia (SCORE Revisão)
80726260016Instrumental Joelho - Prótese Unicompartimental (UNI SCORE) - Versão Navegada
80726260017Source: ANVISA open data, medical device file, updated daily. The public database provides registration validity, rather than registration status: this registration may have been cancelled before its expiry date without this being shown here. Before making purchasing, import or marketing decisions, check the ANVISA search portal.
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