ANVISA registration 82024000017Valid until Mar 23, 2036Endoscopic electrosurgical electrode, bipolar, single use
ANVISA Registration Number: 82024000017NEXON MEDTECH INDUSTRIA E COMERCIO DE PRODUTOS PARA SAUDE LTDANEXON MEDTECH INDUSTRIA E COMERCIO DE PRODUTOS PARA SAUDE LTDARisk Class III
Device names
- Technical name
- Endoscopic electrosurgical electrode, bipolar, single use
- Risk class
- Class III
PT: Eletrodo eletrocirúrgico endoscópico, bipolar, uso único
Registration details
- Registration Number
- 82024000017
- Process Number
- 25351238751202512
- CNPJ
- 34594057000188
Company information
- Registration Holder
- NEXON MEDTECH INDUSTRIA E COMERCIO DE PRODUTOS PARA SAUDE LTDA
- Manufacturing Country
- Brazil
PT: BRASIL
Dates and status
- Publication Date
- Mar 23, 2026
- Validity
- 23/03/2036
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for Endoscopic electrosurgical electrode, bipolar, single use in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 82024000017 and manufactured by NEXON MEDTECH INDUSTRIA E COMERCIO DE PRODUTOS PARA SAUDE LTDA. The registration is held by NEXON MEDTECH INDUSTRIA E COMERCIO DE PRODUTOS PARA SAUDE LTDA with validity until Mar 23, 2036.
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.