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ANVISA registration 81692610290Active

SELF-TEST INSTRUMENT FOR GLUCOSE, URIC ACID AND KETONE BODIES

ANVISA Registration Number: 81692610290VYTTRA DIAGNOSTICOS S.A.VIVACHEK BIOTECH (HANGZHOU) CO., LTD.Risk Class III
Verified
Device names
Technical name
SELF-TEST INSTRUMENT FOR GLUCOSE, URIC ACID AND KETONE BODIES
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PT: INSTRUMENTO AUTOTESTE PARA GLICOSE, ÁCIDO ÚRICO E CORPOS CETÔNICOS
Commercial name
Familia Proxima ALIVE Multi
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Risk class
Class III
Registration details
Registration Number
81692610290
Process Number
25351652170202310
CNPJ
00904728001209
Company information
Registration Holder
VYTTRA DIAGNOSTICOS S.A.
Manufacturer
VIVACHEK BIOTECH (HANGZHOU) CO., LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Jun 03, 2024
Status
Active
Last Updated
08/19/2026 19:00:01
About this record

Access comprehensive regulatory information for SELF-TEST INSTRUMENT FOR GLUCOSE, URIC ACID 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 81692610290 and manufactured by VIVACHEK BIOTECH (HANGZHOU) CO., LTD.. The registration is held by VYTTRA DIAGNOSTICOS S.A. with validity until Jun 03, 2034.

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.