COAGULATION FACTOR XIII - ANVISA Registration 80102511690

Access comprehensive regulatory information for COAGULATION FACTOR XIII in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80102511690 and manufactured by KAMIYA BIOMEDICAL COMPANY. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including DIAGNOSTICA STAGO S.A.S., TECHNOCLONE HERSTELLUNG VON DIAGNOSTIKA UND ARZNEIMITTEL GMBH, 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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80102511690
Registration Details
ANVISA Registration Number: 80102511690
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

FAMÍLIA K-ASSAY® FACTOR XIII
Risk Class II

Registration Details

80102511690

25351911780201629

04718143000194

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Sep 19, 2016

VIGENTE

09/18/2025 19:00:01