D-DIMER - ANVISA Registration 80132390013
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 80132390013 and manufactured by Continental produtos biologicos ltda. The registration is held by CONTINENTAL PRODUTOS BIOLOGICOS LTDA with validity until Aug 09, 2031.
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, 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.

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Registration Details
80132390013
25351656673202101
61058400000142
Company Information
Dates and Status
Aug 09, 2021
09/08/2031
09/18/2025 19:00:01
D-DIMER
Família DIMER ONE
Continental produtos biologicos ltda
80132390005
Oct 26, 2020
D-DIMER
Família D-Dimer
Not specified
80254180457
Nov 21, 2022
D-DIMER
FAMÍLIA D-DIMER
Not specified
10287411357
Sep 10, 2018
D-DIMER
Família D-Dimer
THERMO FISHER SCIENTIFIC OY
80254180457
Nov 21, 2022
D-DIMER
FAMÍLIA D-DIMER
ROCHE DIAGNOSTICS GMBH
10287411357
Sep 10, 2018
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