ANVISA registration

LUMII, LUMII PRO, LUMILIGHT e LUMILIGHT PRO

Registration 80571459011. Aparelho de Multiplo Uso em Estetica

Registration details

Registration number80571459011
Application number25351374071202472
Technical nameAparelho de Multiplo Uso em Estetica
Risk classII
Published on09/09/2024
ValidityIndefinite validity

Registration holder

Legal nameFISMATEK INDÚSTRIA E COMÉRCIO LTDA - ME
CNPJ55.532.188/0001-00

Manufacturer

  • BEIJING ADSS DEVELOPMENT CO., LTD. CHINA, REPÚBLICA POPULAR

Other registrations held by FISMATEK INDÚSTRIA E COMÉRCIO LTDA - MEview all

CLINIX RY580 e CLINIX RY580 PRO

80571450002

REVERSI

80571450003

VELLIX

80571450004

VACUODERMO FISMATEK

80571459002

Vacuodermo Led

80571459003

Onix

80571459004

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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