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 DIAGNรSTICA 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.
Related Devices (2)
Registration Details
10287411743
25351448997202410
30280358000186
Company Information
Dates and Status
Apr 07, 2025
07/04/2035
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 PD-L1 (SP263) Assay
VENTANA MEDICAL SYSTEM, INC
10287411301
Feb 14, 2018
COMPANION DIAGNOSTICS
VENTANA PD-L1 (SP263) Assay
Not specified
10287411301
Feb 14, 2018
COMPANION DIAGNOSTICS
VENTANA PD-L1 (SP142) Assay
ROCHE DIAGNOSTICS GMBH
10287411206
Mar 13, 2017

