HISTOCOMPATIBILITY PRODUCTS - HLA SEROLOGICAL : FLOW CYTOMETRY - ANTIBODY STUDY BY FLOW CYTOMETRY - ANVISA Registration 80391910001

Access comprehensive regulatory information for HISTOCOMPATIBILITY PRODUCTS - HLA SEROLOGICAL : FLOW CYTOMETRY - ANTIBODY STUDY BY FLOW CYTOMETRY in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80391910001 and manufactured by IMMUCOR GTI DIAGNOSTICS, INC. The registration is held by PH 7 COMÉRCIO E REPRESENTAÇÕES DE PRODUTOS PARA DIAGNÓSTICOS LTDA with validity until May 18, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 2 companies making the same product including ONE LAMBDA, INC., IMMUCOR GTI DIAGNOSTICS, INC, and 4 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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Registration Details
ANVISA Registration Number: 80391910001
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Registration Details

80391910001

25351044725200924

59920132000184

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

May 18, 2009

18/05/2034

09/18/2025 19:00:01

Registration Details

80391910001

25351044725200924

59920132000184

Dates and Status

May 18, 2009

18/05/2034

09/18/2025 19:00:01

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