FERRITIN - TUMOR MARKER - ANVISA Registration 10009010428
Access comprehensive regulatory information for FERRITIN - TUMOR MARKER in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10009010428 and manufactured by LABTEST DIAGNOSTICA S/A. The registration is held by LABTEST DIAGNOSTICA S/A with validity until Feb 24, 2035.
This page provides complete technical specifications for this device, regulatory compliance details, 3 companies making the same product including DIASORIN ITALIA S.P.A., SHENZHEN NEW INDUSTRIES BIOMEDICAL ENGINEERING CO., LTD., 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.
Device Details
Registration Details
10009010428
25351883707202391
16516296000138
Company Information
Dates and Status
Jan 22, 2024
24/02/2035
09/18/2025 19:00:01
FERRITINA - MARCADOR TUMORAL
Familia LIAISON® Ferritina
DIASORIN ITALIA S.P.A.
10339840564
Aug 04, 2025
FERRITINA - MARCADOR TUMORAL
Familia LIAISON® Ferritina
Not specified
10339840564
Aug 04, 2025
FERRITINA - MARCADOR TUMORAL
Família AutoLumo Ferritina Micropartículas (CLIA)
AUTOBIO DIAGNOSTICS CO., LTD
80102513310
Oct 21, 2024
FERRITINA - MARCADOR TUMORAL
Família AutoLumo Ferritina Micropartículas (CLIA)
Not specified
80102513310
Oct 21, 2024
FERRITINA - MARCADOR TUMORAL
Família Maglumi Ferritina (CLIA)
Not specified
80102513288
Sep 02, 2024

