ANVISA registration

ENLIGHT 2100

Registration 81408229004. Pletismografo

Registration details

Registration number81408229004
Application number25351166075202217
Technical namePletismografo
Risk classII
Published on25/03/2022
ValidityIndefinite validity

Registration holder

Legal nameTimpel S.A.
CNPJ06.370.174/0002-03

Manufacturer

  • TIMPEL S.A. BRASIL

Other registrations held by Timpel S.A.view all

Cinta ENLIGHT

81408220001

CABO ADAPTADOR

81408220002

CABO DE REFERÊNCIA PACIENTE

81408220003

enlight addere

81408220005

Addere

81408220006

Adapter Cable

81408220007

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