17-HYDROXYPROGESTERONE (17-OHP) - ANVISA Registration 10009010499

Access comprehensive regulatory information for 17-HYDROXYPROGESTERONE (17-OHP) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10009010499 and manufactured by VIRTUE DIAGNOSTICS SUZHOU CO. LTD.. The registration is held by LABTEST DIAGNOSTICA S/A with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including DIAMETRA SRL, DRG INSTRUMENTS GMBH, 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
10009010499
Registration Details
ANVISA Registration Number: 10009010499
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

Device Details

17-a- Hydroxyprogesterone Reagent Kit
Risk Class II

Registration Details

10009010499

25351108686202593

16516296000138

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Aug 18, 2025

VIGENTE

09/18/2025 19:00:01