DEVICE FOR DIAGNOSIS - ANVISA Registration 10275160049

Access comprehensive regulatory information for DEVICE FOR DIAGNOSIS in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 10275160049 and manufactured by HEMEDEX INC. The registration is held by SUPORTE HOSPITALAR LTDA with validity until Oct 24, 2026.

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 MADHU INSTRUMENTS PVT. LTD, LEEDSAY S/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 Similar Products
5 Competitors
10275160049
2 Related Devices
Registration Details
ANVISA Registration Number: 10275160049
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)

QFlow 500 Titanium Bolt - Single Lumen Bolt Kit
Risk Class IV

Registration Details

10275160049

25351830913201609

73857393000128

Company Information

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

Dates and Status

Oct 24, 2016

24/10/2026

09/18/2025 19:00:01

QFlow 500 Titanium Bolt - Single Lumen Bolt Kit
Risk Class IV

Registration Details

10275160049

25351830913201609

73857393000128

Company Information

Dates and Status

Oct 24, 2016

24/10/2026

09/18/2025 19:00:01