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ANVISA registration 80812770025Active

CREATININE

ANVISA Registration Number: 80812770025MEX GLOBAL EQUIPAMENTOS PARA DIAGNÓSTICOS LTDAARKRAY FACTORY, INC.Risk Class II
Verified
Device names
Technical name
CREATININE
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PT: CREATININA
Commercial name
SPOTCHEM II Creatinine
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Risk class
Class II
Registration details
Registration Number
80812770025
Process Number
25351865031201673
CNPJ
11098622000110
Company information
Registration Holder
MEX GLOBAL EQUIPAMENTOS PARA DIAGNÓSTICOS LTDA
Manufacturer
ARKRAY FACTORY, INC.
Manufacturing Country
Japan
PT: JAPÃO
Dates and status
Publication Date
Jul 18, 2016
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for CREATININE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80812770025 and manufactured by ARKRAY FACTORY, INC.. The registration is held by MEX GLOBAL EQUIPAMENTOS PARA DIAGNÓSTICOS LTDA with validity until currently active (VIGENTE).

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.