Self-test instrument for glucose and ketone bodies - ANVISA Registration 80117581216

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 80117581216 and manufactured by APEX BIOTECHNOLOGY CORPORATION. The registration is held by EMERGO BRAZIL IMPORT IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS HOSPITALARES LTDA with validity until Mar 31, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 1 companies making the same product including 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: 80117581216
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Related Devices (2)

MultiSure GK Sistema de monitoramento de glicose e cetona no sangue
Risk Class III

Registration Details

80117581216

25351426022202422

04967408000198

Company Information

Dates and Status

Mar 31, 2025

31/03/2035

09/18/2025 19:00:01

MultiSure GK Sistema de monitoramento de glicose e cetona no sangue
Risk Class III

Registration Details

80117581216

25351426022202422

04967408000198

Dates and Status

Mar 31, 2025

31/03/2035

09/18/2025 19:00:01

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