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Mobile X-Ray Machine - ANVISA Registration 80101380025

Access comprehensive regulatory information for Mobile 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 80101380025 and manufactured by manufacturer not specified. The registration is held by KONICA MINOLTA HEALTHCARE DO BRASIL INDUSTRIA DE EQUIPAMENTOS MEDICOS LTDA with validity until Aug 19, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including SIEMENS HEALTHCARE GMBH, FUJIFILM 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.

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80101380025
2 Related Devices
Registration Details
ANVISA Registration Number: 80101380025
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Related Devices (2)

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Registration Details

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71256283000185

Dates and Status

Aug 19, 2024

19/08/2034

09/18/2025 19:00:01

AeroDR Maxmove
Risk Class III

Registration Details

80101380025

25351354162202491

71256283000185

Dates and Status

Aug 19, 2024

19/08/2034

09/18/2025 19:00:01