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ANVISA registration 81816720094Active

COAGULATION FACTOR VIII

ANVISA Registration Number: 81816720094ALIFAX BRASIL COMER., EXP., IMP., DIST. DE EQUIPAMENTOS E REAGENTES PARA DIAGNOSTICO IN VITRO LTDATECHNOCLONE HERSTELLUNG VON DIAGNOSTIKA UND ARZNEIMITTEL GMBHRisk Class II
Verified
Device names
Technical name
COAGULATION FACTOR VIII
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PT: FATOR VIII DE COAGULAÇÃO
Commercial name
Technochrom FVIII:C 2G
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Risk class
Class II
Registration details
Registration Number
81816720094
Process Number
25351088716202619
CNPJ
31167508000102
Company information
Registration Holder
ALIFAX BRASIL COMER., EXP., IMP., DIST. DE EQUIPAMENTOS E REAGENTES PARA DIAGNOSTICO IN VITRO LTDA
Manufacturer
TECHNOCLONE HERSTELLUNG VON DIAGNOSTIKA UND ARZNEIMITTEL GMBH
Manufacturing Country
Austria
PT: ÁUSTRIA
Dates and status
Publication Date
Jun 15, 2026
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for COAGULATION FACTOR VIII in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81816720094 and manufactured by TECHNOCLONE HERSTELLUNG VON DIAGNOSTIKA UND ARZNEIMITTEL GMBH. The registration is held by ALIFAX BRASIL COMER., EXP., IMP., DIST. DE EQUIPAMENTOS E REAGENTES PARA DIAGNOSTICO IN VITRO 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.