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

Instrument Kit - ANVISA Registration 80455639016

Access comprehensive regulatory information for Instrument Kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80455639016 and manufactured by TRAUMEC TECNOLOGIA E IMPLANTES ORTOPÉDICOS IMP. E EXP. LTDA - EPP. The registration is held by TRAUMEC TECNOLOGIA E IMPLANTES ORTOPÉDICOS IMP. E EXP. LTDA - EPP with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 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 Competitors
5 Recent Registrations
80455639016
Registration Details
ANVISA Registration Number: 80455639016
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Kit Instrumental para CranialFlex Traumec
Risk Class II

Registration Details

80455639016

25351412886202467

09123223000110

Dates and Status

Oct 07, 2024

VIGENTE

09/18/2025 19:00:01