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BONE GRAFT AND ASSOCIATED DEVICES - ANVISA Registration 80202250001

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 80202250001 and manufactured by BERKELEY ADVANCED BIOMATERIALS. The registration is held by ORTHONEURO COMÉRCIO IMPORTAÇÃO E EXPORTAÇÃO DE PRODUTOS MÉDICOS S/A with validity until Oct 17, 2025.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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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80202250001
2 Related Devices
Registration Details
ANVISA Registration Number: 80202250001
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Related Devices (2)

Enxerto Cem Ostetic™ Putty
Risk Class IV
Expired

Registration Details

80202250001

25351127592200570

04886535000162

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Oct 17, 2005

17/10/2025

09/18/2025 19:00:01

Enxerto Cem Ostetic™ Putty
Risk Class IV
Expired

Registration Details

80202250001

25351127592200570

04886535000162

Dates and Status

Oct 17, 2005

17/10/2025

09/18/2025 19:00:01