Pure Global

Instrument for nucleic acid analysis - ANVISA Registration 80144950539

Access comprehensive regulatory information for Instrument for nucleic acid analysis in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80144950539 and manufactured by BIONEER CORPORATION. The registration is held by REM INDUSTRIA E COMERCIO LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including ROCHE MOLECULAR SYSTEMS, INC, QIAGEN 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
5 Competitors
5 Recent Registrations
80144950539
Registration Details
ANVISA Registration Number: 80144950539
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Registration Details

80144950539

25351476278201602

47334701000120

Company Information

South Korea
PT: CORÉIA DO SUL

Dates and Status

Mar 06, 2017

VIGENTE

09/18/2025 19:00:01