Regenerative Membranes - ANVISA Registration 80255120001

Access comprehensive regulatory information for Regenerative Membranes in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80255120001 and manufactured by BIONEXT PRODUTOS BIOTECNOLOGICOS LTDA. The registration is held by BIONEXT PRODUTOS BIOTECNOLOGICOS LTDA with validity until Jan 09, 2036.

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 INTEGRA LIFESCIENCES CORPORATION, INTEGRA LIFESCIENCES CORPORATION (PRINCETON), 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
80255120001
Registration Details
ANVISA Registration Number: 80255120001
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

BIONEXT - CURATIVO BARREIRA MECÂNICA PARA FERIDAS
Risk Class III

Registration Details

80255120001

25351298083200521

05423767000147

Company Information

Brazil
PT: BRASIL

Dates and Status

Jan 09, 2006

09/01/2036

09/18/2025 19:00:01