Biopsy Device - ANVISA Registration 80471700028

Access comprehensive regulatory information for Biopsy Device in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80471700028 and manufactured by Geotek Medikal ve Saglik Hizmetleri Tic.San.Ltd.Sti. The registration is held by BRASMED SUL ODONTO-HOSPITALAR LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including STERYLAB S.R.L., Zamar D.O.O., 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 Similar Products
5 Competitors
80471700028
Registration Details
ANVISA Registration Number: 80471700028
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

🇧🇷 Brazil Regulatory Expert

Need help with your Brazil registration?

Contact Pure Global Brazil Team
Free consultation

Device Details

DISPOSITIVO MAXICORE-U
Risk Class II

Registration Details

80471700028

25351006596201911

08918717000129

Company Information

Turkey
PT: TURQUIA

Dates and Status

Mar 25, 2019

VIGENTE

09/18/2025 19:00:01