Self-test instrument for glucose and ketone bodies - ANVISA Registration 80146501903

Access comprehensive regulatory information for Self-test instrument for glucose and ketone bodies in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80146501903 and manufactured by ABBOTT DIABETES CARE LTD. The registration is held by ABBOTT LABORATORIOS DO BRASIL LTDA with validity until Nov 24, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 2 companies making the same product including APEX BIOTECHNOLOGY CORPORATION, ABBOTT DIABETES CARE LTD, and 4 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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Registration Details
ANVISA Registration Number: 80146501903
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

FREESTYLE LIBRE FLASH GLUCOSE MONITORING SYSTEM/ FREESTYLE LIBRE SIST FLASH DE MONITOR DE GLICOSE
Risk Class III

Registration Details

80146501903

25351405133201439

56998701000116

Company Information

United Kingdom
PT: REINO UNIDO

Dates and Status

Nov 24, 2014

24/11/2034

09/18/2025 19:00:01

FREESTYLE LIBRE FLASH GLUCOSE MONITORING SYSTEM/ FREESTYLE LIBRE SIST FLASH DE MONITOR DE GLICOSE
Risk Class III

Registration Details

80146501903

25351405133201439

56998701000116

Company Information

Dates and Status

Nov 24, 2014

24/11/2034

09/18/2025 19:00:01

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