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X-Ray Intensifying Screen - ANVISA Registration 10410130030

Access comprehensive regulatory information for X-Ray Intensifying Screen in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10410130030 and manufactured by UNIRAY MEDICAL LLP. The registration is held by CONTROLLER COMÉRCIO E SERVIÇOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 1 companies making the same product including KIRAN MEDICAL SYSTEMS, and 2 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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10410130030
Registration Details
ANVISA Registration Number: 10410130030
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Device Details

TELA INTENSIFICADORA DE RAIO-X (VERDE) LUMAX
Risk Class II

Registration Details

10410130030

25351503444201708

78515210000100

Company Information

UNIRAY MEDICAL LLP
India
PT: ÍNDIA

Dates and Status

Oct 31, 2017

VIGENTE

09/18/2025 19:00:01

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