COAGULATION FACTOR IV - ANVISA Registration 80003610568

Access comprehensive regulatory information for COAGULATION FACTOR IV in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80003610568 and manufactured by BIOKIT S/A. The registration is held by WERFEN MEDICAL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 1 companies making the same product including DIAGNOSTICA STAGO S.A.S., and 1 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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80003610568
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Registration Details
ANVISA Registration Number: 80003610568
Janaina dos Santos de Miranda

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Related Devices (2)

Família HemosIL HIT-Ab
Risk Class II

Registration Details

80003610568

25351077639201942

02004662000165

Company Information

BIOKIT S/A
Spain
PT: ESPANHA

Dates and Status

Apr 08, 2019

VIGENTE

09/18/2025 19:00:01

Família HemosIL HIT-Ab
Risk Class II

Registration Details

80003610568

25351077639201942

02004662000165

Company Information

BIOKIT SA
Spain
PT: ESPANHA

Dates and Status

Apr 08, 2019

VIGENTE

09/18/2025 19:00:01

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Recent Registrations
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