Pure Global

COMPANION DIAGNOSTICS - ANVISA Registration 10287411745

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 10287411745 and manufactured by manufacturer not specified. The registration is held by ROCHE DIAGNร“STICA BRASIL LTDA with validity until May 05, 2035.

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.

Free Database
Powered by Pure Global AI
100,000+ Devices
3 Competitors
5 Recent Registrations
10287411745
2 Related Devices
Registration Details
ANVISA Registration Number: 10287411745
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Related Devices (2)

Anti-ALK (D5F3) Rabbit Monoclonal Primary
Risk Class III

Registration Details

10287411745

25351027352202510

30280358000186

Company Information

Dates and Status

May 05, 2025

05/05/2035

09/18/2025 19:00:01

Anti-ALK (D5F3) Rabbit Monoclonal Primary
Risk Class III

Registration Details

10287411745

25351027352202510

30280358000186

Company Information

Germany
PT: ALEMANHA

Dates and Status

May 05, 2025

05/05/2035

09/18/2025 19:00:01