Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

Regenerative Membranes - ANVISA Registration 80117580851

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 80117580851 and manufactured by AROA BIOSURGERY LTD. The registration is held by EMERGO BRAZIL IMPORT IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS HOSPITALARES LTDA with validity until Dec 23, 2029.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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 Competitors
5 Recent Registrations
80117580851
2 Related Devices
Registration Details
ANVISA Registration Number: 80117580851
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Related Devices (2)

Endoform Antimicrobial Restorative Bioscaffold
Risk Class IV

Registration Details

80117580851

25351263742201911

04967408000198

Company Information

New Zealand
PT: NOVA ZELÂNDIA

Dates and Status

Dec 23, 2019

23/12/2029

09/18/2025 19:00:01

Endoform Antimicrobial Restorative Bioscaffold
Risk Class IV

Registration Details

80117580851

25351263742201911

04967408000198

Dates and Status

Dec 23, 2019

23/12/2029

09/18/2025 19:00:01