Self-test instrument for glucose - ANVISA Registration 10410130024

Access comprehensive regulatory information for Self-test instrument for glucose in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10410130024 and manufactured by manufacturer not specified. The registration is held by CONTROLLER COMÉRCIO E SERVIÇOS LTDA with validity until Oct 13, 2035.

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 OK BIOTECH CO., LTD., TIANJIN EMPECS MEDICAL DEVICE CO. LTD, 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
10410130024
2 Related Devices
Registration Details
ANVISA Registration Number: 10410130024
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)

MONITOR DE GLICOSE BIOLAND G-500
Risk Class III

Registration Details

10410130024

25351664497201498

78515210000100

Company Information

Dates and Status

Oct 13, 2015

13/10/2035

09/18/2025 19:00:01

MONITOR DE GLICOSE BIOLAND G-500
Risk Class III

Registration Details

10410130024

25351664497201498

78515210000100

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Oct 13, 2015

13/10/2035

09/18/2025 19:00:01