ANVISA registration

Fio Guia revestido de PTFE

Registration 10256400061. Fio Guia

Registration details

Registration number10256400061
Application number25351223531201938
Technical nameFio Guia
Risk classII
Published on03/06/2019
ValidityIndefinite validity

Registration holder

Legal nameBIOMEDICAL PRODUTOS CIENTIFICOS MEDICOS E HOSPITALARES S A
CNPJ19.848.316/0001-66

Manufacturer

  • SHANGHAI KINDLY MEDICAL INSTRUMENTS CO., LTD CHINA, REPÚBLICA POPULAR

Other registrations held by BIOMEDICAL PRODUTOS CIENTIFICOS MEDICOS E HOSPITALARES S Aview all

CATETER PARA EMBOLECTOMIA LUCAS MEDICAL

10256400006

CATETER DIAGNOSTICO ANGIOGRAFICO RADIOLOGICO

10256400022

CATETER ELETRODO TEMPORARIO

10256400025

ENXERTO VASCULAR COM COLÁGENO V.U.P.

10256400036

Bainha Dilatadora TightRail

10256400040

Pulseira de Compressão BIRD

10256400041

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