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LEGIONELLA - ANVISA Registration 10225960034

Access comprehensive regulatory information for LEGIONELLA in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10225960034 and manufactured by SCIMEDX CORP. The registration is held by MEDIVAX INDÚSTRIA E COMÉRCIO 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 VIRCELL S.L., QUIDEL 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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10225960034
Registration Details
ANVISA Registration Number: 10225960034
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Device Details

LEGIONELLA DFA
Risk Class II

Registration Details

10225960034

253510002010266

68814961000173

Company Information

SCIMEDX CORP
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Aug 16, 2002

VIGENTE

09/18/2025 19:00:01