Regenerative Membranes - ANVISA Registration 10306840095

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 10306840095 and manufactured by INTEGRA LIFESCIENCES CORPORATION. The registration is held by PROMEDON DO BRASIL PRODUTOS MEDICO HOSPITALARES LTDA with validity until Jan 28, 2028.

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 (PRINCETON), M3 Health Indústria e Comércio de Produtos Médicos, Odontológicos e Correlatos S.A., 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.

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10306840095
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Registration Details
ANVISA Registration Number: 10306840095
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

MATRIZ DE REGENARACAO DURAL DURAGEN PLUS
Risk Class IV

Registration Details

10306840095

25351425356200605

00028682000140

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jan 28, 2008

28/01/2028

09/18/2025 19:00:01

MATRIZ DE REGENARACAO DURAL DURAGEN PLUS
Risk Class IV

Registration Details

10306840095

25351425356200605

00028682000140

Company Information

Dates and Status

Jan 28, 2008

28/01/2028

09/18/2025 19:00:01