SELF-TEST FOR GLUCOSE - ANVISA Registration 80102513043

Access comprehensive regulatory information for SELF-TEST FOR GLUCOSE in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80102513043 and manufactured by TIANJIN EMPECS MEDICAL DEVICE CO. LTD. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Jul 03, 2033.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including OK BIOTECH CO., LTD., ROCHE DIABETES CARE GMBH, 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.

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80102513043
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Registration Details
ANVISA Registration Number: 80102513043
Janaina dos Santos de Miranda

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Related Devices (2)

Família de Teste de Glicose Sanguínea G-TECH Vita
Risk Class III

Registration Details

80102513043

25351149165202324

04718143000194

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jul 03, 2023

03/07/2033

09/18/2025 19:00:01

Família de Teste de Glicose Sanguínea G-TECH Vita
Risk Class III

Registration Details

80102513043

25351149165202324

04718143000194

Dates and Status

Jul 03, 2023

03/07/2033

09/18/2025 19:00:01