ANVISA registration

RESTYLANE SKINBOOSTERS LIDOCAINE

Registration 80251760007. Solucao para Preenchimento Intradermico

Registration details

Registration number80251760007
Application number25351255630201499
Technical nameSolucao para Preenchimento Intradermico
Risk classIV
Published on25/01/2016
ValidityValid until 25/01/2036

Registration holder

Legal nameGALDERMA BRASIL LTDA
CNPJ00.317.372/0001-46

Manufacturer

  • Q-MED AB SUÉCIA

Other registrations held by GALDERMA BRASIL LTDAview all

RESTYLANE EMERVEL LIDOCAINE

80251760002

RESTYLANE LIDOCAINE

80251760004

Sculptra

80251760008

Restylane

80251760010

Restylane Kysse

80251760013

Restylane Volyme

80251760014

Source: ANVISA

Source: 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