ANVISA registration

SURGI-MAX

Registration 81189660103. Equipamento Cirurgico de Alta Frequencia

Registration details

Registration number81189660103
Application number25351772550202116
Technical nameEquipamento Cirurgico de Alta Frequencia
Risk classIII
Published on06/12/2021
ValidityValid until 27/08/2027

Registration holder

Legal nameSÓLIDA HOSPITALAR - DISTRIBUIDORA DE MATERIAL HOSPITALAR LTDA
CNPJ21.196.966/0001-16

Manufacturer

  • ELLIQUENCE, LLC ESTADOS UNIDOS DA AMÉRICA

Other registrations held by SÓLIDA HOSPITALAR - DISTRIBUIDORA DE MATERIAL HOSPITALAR LTDAview all

CÂNULA DESCARTÁVEL LCCS PARA RIZOTOMIA FACETÁRIA

81189660001

Cânula Discectomia Percutânea Discal Orthozon

81189660002

Cânula para Discectomia Percutânea Discal

81189660003

Fio Guia PTFE

81189660004

Fio Guia Hidrofílico Twister

81189660005

Fio Guia Hidrofílico

81189660006

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