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IMMUNOHEMATOLOGY - ABO - HUMAN ORIGIN - ANVISA Registration 80155020032

Access comprehensive regulatory information for IMMUNOHEMATOLOGY - ABO - HUMAN ORIGIN in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80155020032 and manufactured by programa nacional de controle de qualidade ltda. The registration is held by programa nacional de controle de qualidade ltda with validity until Apr 24, 2033.

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including DIAGNOSTIC GRIFOLS, S.A., DIAGNOSTIC GRIFOLS S.A., and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.

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80155020032
Registration Details
ANVISA Registration Number: 80155020032
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Device Details

Família Controle Interno Grupo Sanguíneo e Fator Rh
Risk Class IV

Registration Details

80155020032

25351560099202269

73302879000108

Company Information

Brazil
PT: BRASIL

Dates and Status

Apr 24, 2023

24/04/2033

09/18/2025 19:00:01