ANVISA registration
Puregraft 250/850
Registration 80588390003. Bolsa Para Reinfusao
Registration details
| Registration number | 80588390003 |
|---|---|
| Application number | 25351060418201701 |
| Technical name | Bolsa Para Reinfusao |
| Risk class | II |
| Published on | 27/03/2017 |
| Validity | Indefinite validity |
Registration holder
| Legal name | ESTABLISHMENT LABS BRASIL PRODUTOS PARA SAUDE LTDA |
|---|---|
| CNPJ | 08.290.164/0001-02 |
Manufacturer
- Puregraft LLC ESTADOS UNIDOS DA AMÉRICA
Other registrations held by ESTABLISHMENT LABS BRASIL PRODUTOS PARA SAUDE LTDAview all
Moldes Intraoperatórios para Prótese Mamária - Estéril
80588390001IMPLANTE MAMÁRIO Motiva Implant Matrix® with Qid
80588390002IMPLANTE MAMÁRIO Motiva Implant Matrix® without Qid
80588390004GLUTEALARMONIC SILKSURFACE MOTIVA IMPLANTS MATRIX - IMPLANTES ESTEREIS DE SILICONE PARA GLÚTEOS
80588390005MotivaHybrid Bulb cannula kit
80588390006MotivaImagine - Insertion Sleeve
80588390007Source: 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.
Next step
Medical device registration with ANVISA
HSC manages the process from risk classification to liaising with the regulator, in Brazil and more than 40 other countries.
Speak to a specialist