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ANVISA registration 10303460488Active

LYSIS SOLUTION

ANVISA Registration Number: 10303460488IN VITRO DIAGNOSTICA LTDAHUMAN GMBHRisk Class I
Verified
Device names
Technical name
LYSIS SOLUTION
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PT: SOLUÇÃO DE LISE
Commercial name
HC5D CBC Lyse
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Risk class
Class I
Registration details
Registration Number
10303460488
Process Number
25351441949201925
CNPJ
42837716000198
Company information
Registration Holder
IN VITRO DIAGNOSTICA LTDA
Manufacturer
HUMAN GMBH
Manufacturing Country
Germany
PT: ALEMANHA
Dates and status
Publication Date
Aug 08, 2019
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for LYSIS SOLUTION in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10303460488 and manufactured by HUMAN GMBH. The registration is held by IN VITRO DIAGNOSTICA 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.