LOW DENSITY LIPOPROTEIN (LDL) - ANVISA Registration 80146502152

Access comprehensive regulatory information for LOW DENSITY LIPOPROTEIN (LDL) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80146502152 and manufactured by SEKISUI DIAGNOSTICS P.E.I. INC. The registration is held by ABBOTT LABORATORIOS DO BRASIL 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 ELITECH CLINICAL SYSTEMS SAS, BIOSYSTEMS S.A., 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
80146502152
Registration Details
ANVISA Registration Number: 80146502152
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

Alinity c Direct LDL Reagent Kit
Risk Class II

Registration Details

80146502152

25351278696201866

56998701000116

Company Information

Canada
PT: CANADÁ

Dates and Status

Jul 16, 2018

VIGENTE

09/18/2025 19:00:01