Regenerative Membranes - ANVISA Registration 10008530068

Access comprehensive regulatory information for Regenerative Membranes in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 10008530068 and manufactured by AESCULAP AG. The registration is held by LABORATORIOS B. BRAUN S/A with validity until Jun 07, 2026.

This page provides complete technical specifications for 2 related devices, 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
10008530068
2 Related Devices
Registration Details
ANVISA Registration Number: 10008530068
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

Related Devices (2)

NEURO-PATCH - MEMBRANAS MICROPOROSAS PARA SUBSTITUIÇÃO DA DURAMATER
Risk Class IV

Registration Details

10008530068

250000056149670

31673254000102

Company Information

AESCULAP AG
Germany
PT: ALEMANHA

Dates and Status

Jun 07, 1996

07/06/2026

09/18/2025 19:00:01

NEURO-PATCH - MEMBRANAS MICROPOROSAS PARA SUBSTITUIÇÃO DA DURAMATER
Risk Class IV

Registration Details

10008530068

250000056149670

31673254000102

Company Information

Dates and Status

Jun 07, 1996

07/06/2026

09/18/2025 19:00:01