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

External Fixation System - ANVISA Registration 80005430725

Access comprehensive regulatory information for External Fixation System in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80005430725 and manufactured by WRIGHT MEDICAL TECHNOLOGY , INC .. The registration is held by STRYKER DO BRASIL LTDA 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 RESPONSE ORTHO TEKNOLOJIK URETIM A S, SELAZ INDÚSTRIA E COMÉRCIO DE APARELHOS BIOMECÂNICOS LTDA, 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
80005430725
Registration Details
ANVISA Registration Number: 80005430725
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

SISTEMA FIXADOR DE TUBO SIDEKICK
Risk Class I

Registration Details

80005430725

25351303104202157

02966317000102

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Sep 23, 2021

VIGENTE

09/18/2025 19:00:01