LEGIONELLA - ANVISA Registration 81816720052

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 81816720052 and manufactured by VIRCELL S.L.. The registration is held by ALIFAX BRASIL COMER., EXP., IMP., DIST. DE EQUIPAMENTOS E REAGENTES PARA DIAGNOSTICO IN VITRO LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Similar Products
5 Competitors
81816720052
Registration Details
ANVISA Registration Number: 81816720052
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

🇧🇷 Brazil Regulatory Expert

Need help with your Brazil registration?

Contact Pure Global Brazil Team
Free consultation

Device Details

LEGIONELLA PNEUMOPHILA SG 1-6 VIRCLIA® IgG+IgM MONOTEST
Risk Class II

Registration Details

81816720052

25351480582202341

31167508000102

Company Information

Dates and Status

Aug 21, 2023

VIGENTE

09/18/2025 19:00:01