Pure Global AI
ANVISA registration 80101380015Active

Indirect flat panel x-ray detector

ANVISA Registration Number: 80101380015KONICA MINOLTA HEALTHCARE DO BRASIL INDUSTRIA DE EQUIPAMENTOS MEDICOS LTDAKONICA MINOLTA, INC.Risk Class II
Verified
Device names
Technical name
Indirect flat panel x-ray detector
View exact technical-name matches →
PT: Detector de raios-x de painel plano indireto
Commercial name
Sistema AeroDR
View exact commercial-name matches →
Risk class
Class II
Registration details
Registration Number
80101380015
Process Number
25351933024201647
CNPJ
71256283000185
Company information
Registration Holder
KONICA MINOLTA HEALTHCARE DO BRASIL INDUSTRIA DE EQUIPAMENTOS MEDICOS LTDA
Manufacturer
KONICA MINOLTA, INC.
Manufacturing Country
Japan
PT: JAPÃO
Dates and status
Publication Date
Jun 20, 2016
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Indirect flat panel x-ray detector in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80101380015 and manufactured by KONICA MINOLTA, INC.. The registration is held by KONICA MINOLTA HEALTHCARE DO BRASIL INDUSTRIA DE EQUIPAMENTOS MEDICOS 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.