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AF Equipment for Therapy - ANVISA Registration 80451969015

Access comprehensive regulatory information for AF Equipment for Therapy in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80451969015 and manufactured by SHENZHEN LEAFLIFE TECHNOLOGY CO., LTD.. The registration is held by NUTRIEX IMPORTACAO E EXPORTACAO DE PRODUTOS NUTRICIONAIS E FARMOQUIMICOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 2 companies making the same product including IBRAMED INDÚSTRIA BRASILEIRA DE EQUIPAMENTOS MÉDICOS - LTDA, EUNSUNG GLOBAL CORPORATION, and 3 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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80451969015
Registration Details
ANVISA Registration Number: 80451969015
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Device Details

Rennova Diamond Tech
Risk Class II

Registration Details

80451969015

25351122564202518

06172459000159

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Aug 18, 2025

VIGENTE

09/18/2025 19:00:01

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