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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.

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10246810330
2 Related Devices
Registration Details
ANVISA Registration Number: 10246810330
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Related Devices (2)

D-Dimer
Risk Class III

Registration Details

10246810330

25351135506201906

72807043000194

Company Information

Argentina
PT: ARGENTINA

Dates and Status

Feb 17, 2020

17/02/2030

09/18/2025 19:00:01

D-Dimer
Risk Class III

Registration Details

10246810330

25351135506201906

72807043000194

Company Information

Brazil
PT: BRASIL

Dates and Status

Feb 17, 2020

17/02/2030

09/18/2025 19:00:01