Self-test instrument for glucose - ANVISA Registration 80117580617

Access comprehensive regulatory information for Self-test instrument 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 80117580617 and manufactured by manufacturer not specified. The registration is held by EMERGO BRAZIL IMPORT IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS HOSPITALARES LTDA with validity until Nov 06, 2027.

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., TIANJIN EMPECS MEDICAL DEVICE CO. LTD, 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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80117580617
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Registration Details
ANVISA Registration Number: 80117580617
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Related Devices (2)

FamĂ­lia Sistema de Monitoramento de Glicemia
Risk Class III

Registration Details

80117580617

25351432671201701

04967408000198

Dates and Status

Nov 06, 2017

06/11/2027

09/18/2025 19:00:01

FamĂ­lia Sistema de Monitoramento de Glicemia
Risk Class III

Registration Details

80117580617

25351432671201701

04967408000198

Company Information

Dates and Status

Nov 06, 2017

06/11/2027

09/18/2025 19:00:01