ANVISA registration 81816720093Active

COAGULATION FACTOR VIII

Name: COAGULATION FACTOR VIII — ANVISA registration 81816720093
Creator: TECHNOCLONE HERSTELLUNG VON DIAGNOSTIKA UND ARZNEIMITTEL GMBH
Keywords: COAGULATION FACTOR VIII, FATOR VIII DE COAGULAÇÃO, Technochrom FVIII:C 2G CAL, 81816720093, Risk Class II, ANVISA registration

ANVISA Registration Number: 81816720093ALIFAX 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
Commercial name: Technochrom FVIII:C 2G CAL
Risk class: Class II

Registration details

Registration Number: 81816720093
Process Number: 25351088711202696
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

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 81816720093 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).

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