INSTRUMENT FOR GLUCOSE AND KETONE BODIES – POINT OF CARE TESTING (PROFESSIONAL) - ANVISA Registration 80146501881

Access comprehensive regulatory information for INSTRUMENT FOR GLUCOSE AND KETONE BODIES – POINT OF CARE TESTING (PROFESSIONAL) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80146501881 and manufactured by ABBOTT DIABETES CARE LTD. 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, 2 companies making the same product including ABBOTT DIABETES CARE LTD, NOVA BIOMEDICAL CORPORATION, and 3 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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80146501881
Registration Details
ANVISA Registration Number: 80146501881
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

FREESTYLE PRECISION PRO BLOOD GLUCOSE AND B-KETONE MONITORING METER KIT / SISTEMA DE MONITORIZAÇÃO DE GLICOSE E B-CETONA FREESTYLE PRECISION PRO
Risk Class II

Registration Details

80146501881

25351577227201397

56998701000116

Company Information

United Kingdom
PT: REINO UNIDO

Dates and Status

Jul 07, 2014

VIGENTE

09/18/2025 19:00:01

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