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ADENOVIRUS - ANVISA Registration 82444370260

Access comprehensive regulatory information for ADENOVIRUS in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82444370260 and manufactured by ZHEJIANG ORIENT GENE BIOTECH CO., LTD.. The registration is held by Enzytec Biotecnologia 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 R-BIOPHARM AG, NOVATEC IMMUNDIAGNOSTICA GMBH, 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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82444370260
Registration Details
ANVISA Registration Number: 82444370260
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Device Details

Família Adenovirus Antigen Fluorescence Rapid Test Cassette (Swab)
Risk Class II

Registration Details

82444370260

25351121459202553

07214566000165

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Sep 01, 2025

VIGENTE

09/18/2025 19:00:01