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CANNABINOID - ANVISA Registration 80464810749

Access comprehensive regulatory information for CANNABINOID in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80464810749 and manufactured by VEDALAB. The registration is held by ARGOSLAB DISTRIBUIDORA DE PRODUTOS PARA LABORATÓRIOS 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 ASSURE TECH. HANGZHOU CO., LTD., ORTHO CLINICAL DIAGNOSTICS, 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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80464810749
Registration Details
ANVISA Registration Number: 80464810749
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Device Details

CANNABI-Screen®
Risk Class II

Registration Details

80464810749

25351619254202007

09377976000152

Company Information

VEDALAB
France
PT: FRANÇA

Dates and Status

Dec 17, 2020

VIGENTE

09/18/2025 19:00:01