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ANVISA registration 80459130062Active

Ureteroscope

ANVISA Registration Number: 80459130062MEDICAL BRAZIL IMPORTAÇÃO, EXPORTAÇÃO E COMÉRCIO DE PRODUTOS MÉDICOS LTDAMAXIFLEX, LLCRisk Class II
Verified
Device names
Technical name
Ureteroscope
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PT: Ureteroscópio
Commercial name
Flex XI U
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Risk class
Class II
Registration details
Registration Number
80459130062
Process Number
25351273600201873
CNPJ
09423516000113
Company information
Registration Holder
MEDICAL BRAZIL IMPORTAÇÃO, EXPORTAÇÃO E COMÉRCIO DE PRODUTOS MÉDICOS LTDA
Manufacturer
MAXIFLEX, LLC
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Jun 25, 2018
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Ureteroscope in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80459130062 and manufactured by MAXIFLEX, LLC. The registration is held by MEDICAL BRAZIL IMPORTAÇÃO, EXPORTAÇÃO E COMÉRCIO DE PRODUTOS MÉDICOS LTDA with validity until currently active (VIGENTE).

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.