HIGH-DENSITY LIPOPROTEIN (HDL) - ANVISA Registration 80096210001

Access comprehensive regulatory information for HIGH-DENSITY LIPOPROTEIN (HDL) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80096210001 and manufactured by SEKISUI DIAGNOSTIC, LLC. The registration is held by DIAGNOSTICOS DA AMERICA S.A. 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 LABTEST DIAGNOSTICA S/A, QUIBASA QUÍMICA BÁSICA LTDA, 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
80096210001
Registration Details
ANVISA Registration Number: 80096210001
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

REAGENTE LIQUID N-GENEOUS HDL-COLESTEROL
Risk Class II

Registration Details

80096210001

25351177798200206

61486650000183

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Dec 05, 2002

VIGENTE

09/18/2025 19:00:01