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.
Device Details
Registration Details
80200260020
25351396980202461
05111219000181
Company Information
Dates and Status
Oct 07, 2024
VIGENTE
09/18/2025 19:00:01
INSTRUMENTO (SEM USO DE REAGENTES)
HealthGo Air
HEALTHGO FABRICANTE DE EQUIPAMENTOS MEDICO-ODONTOLOGICOS LTDA
82743450001
Jan 13, 2025
INSTRUMENTO (SEM USO DE REAGENTES)
Famรญlia HEADWAY Breath Test Analyzer
SHENZHEN ZHONGHE HEADWAY BIO-SCI & TECH CO., LTD.
80117580984
Feb 03, 2022
INSTRUMENTO (SEM USO DE REAGENTES)
HEADWAY Helicobacter Pylori Detector
SHENZHEN ZHONGHE HEADWAY BIO-SCI & TECH CO., LTD.
80117580985
Feb 03, 2022
INSTRUMENTO (SEM USO DE REAGENTES)
NIOX VERO
CIRCASSIA AB
80279429012
Oct 29, 2019

