D-DIMER - ANVISA Registration 10246810330
Access comprehensive regulatory information for D-DIMER in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10246810330 and manufactured by WIENER LABORATORIOS S.A.I.C. The registration is held by LABORLAB PRODUTOS PARA LABORATÓRIOS LTDA EPP with validity until Feb 17, 2030.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including ROCHE DIAGNOSTICS GMBH, INSTRUMENTATION LABORATORY, 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.
Related Devices (2)
Registration Details
10246810330
25351135506201906
72807043000194
Company Information
Dates and Status
Feb 17, 2020
17/02/2030
09/18/2025 19:00:01
Registration Details
10246810330
25351135506201906
72807043000194
Company Information
Dates and Status
Feb 17, 2020
17/02/2030
09/18/2025 19:00:01
D-DÍMERO
Luminis FIA D-Dímero
QINGDAO HIGHTOP BIOTECH CO.,LTD.
80474870166
Sep 08, 2025
D-DÍMERO
Luminis FIA D-Dímero
Not specified
80474870166
Sep 08, 2025
D-DÍMERO
BIOCLIN POCT FIA D-DÍMERO
QUIBASA QUÍMICA BÁSICA LTDA
10269360476
Aug 25, 2025
D-DÍMERO
Tina-quant D-Dimer cobas c
Not specified
10287411756
Aug 18, 2025
D-DÍMERO
Tina-quant D-Dimer cobas c
ROCHE DIAGNOSTICS GMBH
10287411756
Aug 18, 2025

