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

LEAD/ELECTRODE FOR DEEP BRAIN ELECTRICAL STIMULATION SYSTEM - ANVISA Registration 10349001273

Access comprehensive regulatory information for LEAD/ELECTRODE FOR DEEP BRAIN ELECTRICAL STIMULATION SYSTEM in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 10349001273 and manufactured by MEDTRONIC INC. The registration is held by AUTO SUTURE DO BRASIL LTDA. with validity until Nov 22, 2031.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including ABBOTT MEDICAL, DIXI MEDICAL, 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
10349001273
2 Related Devices
Registration Details
ANVISA Registration Number: 10349001273
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Related Devices (2)

Registration Details

10349001273

25351635208202128

01645409000128

Company Information

MEDTRONIC INC
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Nov 22, 2021

22/11/2031

09/18/2025 19:00:01

Registration Details

10349001273

25351635208202128

01645409000128

Company Information

Dates and Status

Nov 22, 2021

22/11/2031

09/18/2025 19:00:01