Pure Global AI
ANVISA registration 80101380025Valid until Aug 19, 2034

Multimodality diagnostic X-ray system, mobile

ANVISA Registration Number: 80101380025KONICA MINOLTA HEALTHCARE DO BRASIL INDUSTRIA DE EQUIPAMENTOS MEDICOS LTDASEDECAL - SOCIEDAD ESPANOLA DE ELETROMEDICINA Y CALIDADE S.ARisk Class III
Verified
Device names
Technical name
Multimodality diagnostic X-ray system, mobile
View exact technical-name matches →
PT: Sistema de raios-X de diagnóstico multimodalidade, móvel
Commercial name
AeroDR Maxmove
View exact commercial-name matches →
Risk class
Class III
Registration details
Registration Number
80101380025
Process Number
25351354162202491
CNPJ
71256283000185
Company information
Registration Holder
KONICA MINOLTA HEALTHCARE DO BRASIL INDUSTRIA DE EQUIPAMENTOS MEDICOS LTDA
Manufacturer
SEDECAL - SOCIEDAD ESPANOLA DE ELETROMEDICINA Y CALIDADE S.A
Manufacturing Country
Spain
PT: ESPANHA
Dates and status
Publication Date
Aug 19, 2024
Validity
19/08/2034
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Multimodality diagnostic X-ray system, mobile in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80101380025 and manufactured by SEDECAL - SOCIEDAD ESPANOLA DE ELETROMEDICINA Y CALIDADE S.A. The registration is held by KONICA MINOLTA HEALTHCARE DO BRASIL INDUSTRIA DE EQUIPAMENTOS MEDICOS LTDA with validity until Aug 19, 2034.

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.