COMPANION DIAGNOSTICS - ANVISA Registration 10287411206
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 10287411206 and manufactured by ROCHE DIAGNOSTICS GMBH. The registration is held by ROCHE DIAGNรSTICA BRASIL LTDA with validity until Mar 13, 2027.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 3 companies making the same product including VENTANA MEDICAL SYSTEM, INC, ROCHE DIAGNOSTICS GMBH, 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
10287411206
25351536373201603
30280358000186
Company Information
Dates and Status
Mar 13, 2017
13/03/2027
09/18/2025 19:00:01
COMPANION DIAGNOSTICS
Anti-ALK (D5F3) Rabbit Monoclonal Primary
Not specified
10287411745
May 05, 2025
COMPANION DIAGNOSTICS
Anti-ALK (D5F3) Rabbit Monoclonal Primary
ROCHE DIAGNOSTICS GMBH
10287411745
May 05, 2025
COMPANION DIAGNOSTICS
VENTANA FOLR1 (FOLR-2.1) RxDx Assay
Not specified
10287411743
Apr 07, 2025
COMPANION DIAGNOSTICS
VENTANA FOLR1 (FOLR-2.1) RxDx Assay
VENTANA MEDICAL SYSTEM, INC
10287411743
Apr 07, 2025
COMPANION DIAGNOSTICS
VENTANA PD-L1 (SP263) Assay
VENTANA MEDICAL SYSTEM, INC
10287411301
Feb 14, 2018

