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INSTRUMENT (WITHOUT USE OF REAGENTS) - ANVISA Registration 80117580984

Access comprehensive regulatory information for INSTRUMENT (WITHOUT USE OF REAGENTS) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80117580984 and manufactured by SHENZHEN ZHONGHE HEADWAY BIO-SCI & TECH CO., LTD.. The registration is held by EMERGO BRAZIL IMPORT IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS HOSPITALARES LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 4 companies making the same product including SHENZHEN ZHONGHE HEADWAY BIO-SCI & TECH CO., LTD., GERATHERM MEDICAL LATIN AMERICA LTDA., 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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80117580984
Registration Details
ANVISA Registration Number: 80117580984
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Device Details

Famรญlia HEADWAY Breath Test Analyzer
Risk Class II

Registration Details

80117580984

25351035956202297

04967408000198

Company Information

China
PT: CHINA, REPรšBLICA POPULAR

Dates and Status

Feb 03, 2022

VIGENTE

09/18/2025 19:00:01