Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

Fixed, digital X-ray machine - ANVISA Registration 80101380017

Access comprehensive regulatory information for Fixed, digital X-ray machine in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80101380017 and manufactured by KONICA MINOLTA HEALTHCARE DO BRASIL INDUSTRIA DE EQUIPAMENTOS MEDICOS LTDA. The registration is held by KONICA MINOLTA HEALTHCARE DO BRASIL INDUSTRIA DE EQUIPAMENTOS MEDICOS LTDA with validity until Apr 03, 2027.

This page provides complete technical specifications for this device, regulatory compliance details, 4 companies making the same product including SHIMADZU CORPORATION KYOTO, CANON MEDICAL SYSTEMS CORPORATION, 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
4 Competitors
5 Recent Registrations
80101380017
Registration Details
ANVISA Registration Number: 80101380017
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

CONJUNTO RADIOLร“GICO DIGITAL ALTUS
Risk Class III

Registration Details

80101380017

25351055834201706

71256283000185

Dates and Status

Apr 03, 2017

03/04/2027

09/18/2025 19:00:01