INTRAVASCULAR GUIDE CATHETER - ANVISA Registration 10216710376

Access comprehensive regulatory information for INTRAVASCULAR GUIDE CATHETER in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10216710376 and manufactured by manufacturer not specified. The registration is held by PHILIPS MEDICAL SYSTEMS LTDA with validity until Aug 12, 2029.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including TERUMO CORPORATION, BOSTON SCIENTIFIC CORPORATION - MARLBOROUGH, 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
10216710376
2 Related Devices
Registration Details
ANVISA Registration Number: 10216710376
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

Related Devices (2)

Cateter IVUS rotativo REFINITY ST
Risk Class III

Registration Details

10216710376

25351252622201981

58295213000178

Company Information

Dates and Status

Aug 12, 2019

12/08/2029

09/18/2025 19:00:01

Cateter IVUS rotativo REFINITY ST
Risk Class III

Registration Details

10216710376

25351252622201981

58295213000178

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Aug 12, 2019

12/08/2029

09/18/2025 19:00:01