FERRITIN - ANVISA Registration 80115310202

Access comprehensive regulatory information for FERRITIN in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80115310202 and manufactured by KOVALENT DO BRASIL LTDA. The registration is held by KOVALENT DO BRASIL 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 ROCHE DIAGNOSTICS GMBH, BIOSYSTEMS 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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80115310202
Registration Details
ANVISA Registration Number: 80115310202
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

TOPKAL FERRITINA (4 níveis)
Risk Class II

Registration Details

80115310202

25351533352201294

04842199000156

Company Information

Brazil
PT: BRASIL

Dates and Status

Dec 24, 2012

VIGENTE

09/18/2025 19:00:01