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Indirect flat panel x-ray detector - ANVISA Registration 80101380015

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 provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including IRAY TECHNOLOGY COMPANY LIMITED, SHENZHEN SONTU MEDICAL IMAGING EQUIPMENT CO., LTD, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.

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80101380015
Registration Details
ANVISA Registration Number: 80101380015
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Device Details

Registration Details

80101380015

25351933024201647

71256283000185

Company Information

Japan
PT: JAPรƒO

Dates and Status

Jun 20, 2016

VIGENTE

09/18/2025 19:00:01