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CULTURE MEDIA AND DEVICES FOR ANAEROBE RESEARCH - ANVISA Registration 82195300025

Access comprehensive regulatory information for CULTURE MEDIA AND DEVICES FOR ANAEROBE RESEARCH in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 82195300025 and manufactured by ZHEJIANG QUARK BIOTECHNOLOGY CO., LTD.. The registration is held by PURE LATAM BRAZIL COMERCIO DE PRODUTOS HOSPITALARES 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 BECTON DICKINSON AND COMPANY, REMEL INC., 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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82195300025
Registration Details
ANVISA Registration Number: 82195300025
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Device Details

Família Meio de cultura para anaeróbios (método de fluorescência)
Risk Class I

Registration Details

82195300025

25351136251202539

27939884000109

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Sep 15, 2025

VIGENTE

09/18/2025 19:00:01