D-DIMER - ANVISA Registration 80102513226
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 80102513226 and manufactured by manufacturer not specified. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Apr 08, 2034.
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
80102513226
25351638621202314
04718143000194
Company Information
Dates and Status
Apr 08, 2024
08/04/2034
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

