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 80044680360

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 80044680360 and manufactured by Biomet Trauma. The registration is held by ZIMMER BIOMET 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 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
80044680360
Registration Details
ANVISA Registration Number: 80044680360
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

KIT INSTRUMENTAL OPTILOCK
Risk Class II

Registration Details

80044680360

25351678889201732

02913684000148

Company Information

Biomet Trauma
United States of America
PT: ESTADOS UNIDOS DA AMร‰RICA

Dates and Status

Dec 18, 2017

VIGENTE

09/18/2025 19:00:01