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COMPANION DIAGNOSTICS - ANVISA Registration 10287411743

Access comprehensive regulatory information for COMPANION DIAGNOSTICS in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10287411743 and manufactured by manufacturer not specified. The registration is held by ROCHE DIAGNร“STICA BRASIL LTDA with validity until Apr 07, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 3 companies making the same product including ROCHE DIAGNOSTICS GMBH, VENTANA MEDICAL SYSTEM, INC, 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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10287411743
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Registration Details
ANVISA Registration Number: 10287411743
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Related Devices (2)

VENTANA FOLR1 (FOLR-2.1) RxDx Assay
Risk Class III

Registration Details

10287411743

25351448997202410

30280358000186

Company Information

Dates and Status

Apr 07, 2025

07/04/2035

09/18/2025 19:00:01

VENTANA FOLR1 (FOLR-2.1) RxDx Assay
Risk Class III

Registration Details

10287411743

25351448997202410

30280358000186

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMร‰RICA

Dates and Status

Apr 07, 2025

07/04/2035

09/18/2025 19:00:01