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INSTRUMENT (WITHOUT USE OF REAGENTS) - ANVISA Registration 80200260020

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 80200260020 and manufactured by GERATHERM MEDICAL LATIN AMERICA LTDA.. The registration is held by GERATHERM MEDICAL LATIN AMERICA LTDA. with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 3 companies making the same product including SHENZHEN ZHONGHE HEADWAY BIO-SCI & TECH CO., LTD., HEALTHGO FABRICANTE DE EQUIPAMENTOS MEDICO-ODONTOLOGICOS 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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80200260020
Registration Details
ANVISA Registration Number: 80200260020
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Device Details

Monitor de Fraรงรฃo Exalada de ร“xido Nรญtrico (FeNO)
Risk Class II

Registration Details

80200260020

25351396980202461

05111219000181

Company Information

Brazil
PT: BRASIL

Dates and Status

Oct 07, 2024

VIGENTE

09/18/2025 19:00:01