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X-Ray Films - ANVISA Registration 82533959020

Access comprehensive regulatory information for X-Ray Films in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82533959020 and manufactured by SHENZHEN KENID MEDICAL DEVICES CO., LTD. The registration is held by MR SAUDE 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 CARESTREAM HEALTH INC., 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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82533959020
Registration Details
ANVISA Registration Number: 82533959020
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Device Details

Filme Dry
Risk Class II

Registration Details

82533959020

25351034737202371

26386899000116

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jan 30, 2023

VIGENTE

09/18/2025 19:00:01