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ANVISA registration 80202250039Valid until Apr 13, 2030

LEAD/ELECTRODE FOR DEEP BRAIN ELECTRICAL STIMULATION SYSTEM

ANVISA Registration Number: 80202250039ORTHONEURO COMÉRCIO IMPORTAÇÃO E EXPORTAÇÃO DE PRODUTOS MÉDICOS S/APMT CORPORATIONRisk Class IV
Verified
Device names
Technical name
LEAD/ELECTRODE FOR DEEP BRAIN ELECTRICAL STIMULATION SYSTEM
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PT: CABO/ELETRODO PARA SISTEMA DE ESTIMULAÇÃO ELÉTRICA CEREBRAL PROFUNDA
Commercial name
ELETRODO sEEG DEPTHALON
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Risk class
Class IV
Registration details
Registration Number
80202250039
Process Number
25351240436202032
CNPJ
04886535000162
Company information
Registration Holder
ORTHONEURO COMÉRCIO IMPORTAÇÃO E EXPORTAÇÃO DE PRODUTOS MÉDICOS S/A
Manufacturer
PMT CORPORATION
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Apr 13, 2020
Validity
13/04/2030
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for LEAD/ELECTRODE FOR DEEP BRAIN ELECTRICAL STIMULATION SYSTEM in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80202250039 and manufactured by PMT CORPORATION. The registration is held by ORTHONEURO COMÉRCIO IMPORTAÇÃO E EXPORTAÇÃO DE PRODUTOS MÉDICOS S/A with validity until Apr 13, 2030.

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.