ANVISA registration

MaxMore Spine

Registration 82752290004. Eletrodo eletrocirúrgico endoscópico, bipolar, uso único

Registration details

Registration number82752290004
Application number25351177650202550
Technical nameEletrodo eletrocirúrgico endoscópico, bipolar, uso único
Risk classIII
Published on15/12/2025
ValidityValid until 15/12/2035

Registration holder

Legal nameSurgitec Comércio e Fabricação de Produtos Médicos e Hospitalares Ltda
CNPJ24.684.423/0004-89

Manufacturer

  • Surgitec Comércio e Fabricação de Produtos Médicos e Hospitalares Ltda BRASIL

Other registrations held by Surgitec Comércio e Fabricação de Produtos Médicos e Hospitalares Ltdaview all

MaxMoreSpine Instruments

82752290001

Gold Forceps MaxMore

82752290002

BLUE SPINE

82752290003

Master Scope

82752290005

SPINE SECURE

82752290006

Instrumentais Surgitec Endo Plate

82752290007

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