ANVISA registration

I-PEN® SINGLE USE SENSOR (I-PEN® SUS)

Registration 81770680000. DISPOSITIVO PARA AVALIAÇÃO DA OSMOLARIDADE LACRIMAL

Registration details

Registration number81770680000
Application number25351240214201986
Technical nameDISPOSITIVO PARA AVALIAÇÃO DA OSMOLARIDADE LACRIMAL
Risk classII
Published on13/05/2019
ValidityIndefinite validity

Registration holder

Legal nameDRYCOM COMÉRCIO, IMPORTAÇÃO E DISTRIBUIÇÃO DE PRODUTOS MÉDICOS E HOSPITALARES LTDA
CNPJ28.152.271/0001-81

Manufacturer

  • I-MED PHARMA INC. CANADÁ

Other registrations held by DRYCOM COMÉRCIO, IMPORTAÇÃO E DISTRIBUIÇÃO DE PRODUTOS MÉDICOS E HOSPITALARES LTDAview all

I-PEN® OSMOLARITY SYSTEM

81770680001

E-Eye

81770680002

I RELIEF

81770680003

SM Tube®

81770680004

Ponteiras AB Max

81770680005

Cyclo G6

81770680007

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