BONE GRAFT AND ASSOCIATED DEVICES - ANVISA Registration 81050760132

Access comprehensive regulatory information for BONE GRAFT AND ASSOCIATED DEVICES in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 81050760132 and manufactured by manufacturer not specified. The registration is held by GUSMED DO BRASIL COMERCIO E LOCAÇÃO DE PRODUTOS MEDICOS LTDA - EPP with validity until Jun 13, 2032.

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 GEISTLICH PHARMA AG, 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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81050760132
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Registration Details
ANVISA Registration Number: 81050760132
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Enxerto Ósseo Moldável Biovidro Ativo Biosphere Putty
Risk Class IV

Registration Details

81050760132

25351441306201981

19443457000107

Dates and Status

Jun 13, 2022

13/06/2032

09/18/2025 19:00:01

Enxerto Ósseo Moldável Biovidro Ativo Biosphere Putty
Risk Class IV

Registration Details

81050760132

25351441306201981

19443457000107

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jun 13, 2022

13/06/2032

09/18/2025 19:00:01