ANVISA registration

RESTYLANE LIDOCAINE

Registration 80251760004. Solucao para Preenchimento Intradermico

Registration details

Registration number80251760004
Application number25351451634201461
Technical nameSolucao para Preenchimento Intradermico
Risk classIV
Published on19/01/2015
ValidityValid until 19/01/2035

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 SKINBOOSTERS LIDOCAINE

80251760007

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.

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