Instrument Kit - ANVISA Registration 80203020039

Access comprehensive regulatory information for Instrument Kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80203020039 and manufactured by MAHE MEDICAL GMBH. The registration is held by BONE SURGICAL EQUIPAMENTOS MEDICOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including MARDEN MEDICAL LTDA, LIMA CORPORATE S.P.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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Similar Products
5 Competitors
80203020039
Registration Details
ANVISA Registration Number: 80203020039
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

Device Details

Kit de Fresa Intramedular Flexível
Risk Class I

Registration Details

80203020039

25351509847201579

04408009000197

Company Information

MAHE MEDICAL GMBH
Germany
PT: ALEMANHA

Dates and Status

Oct 05, 2015

VIGENTE

09/18/2025 19:00:01