CREATINE KINASE (CK) - ANVISA Registration 10231810020

Access comprehensive regulatory information for CREATINE KINASE (CK) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10231810020 and manufactured by DOLES REAGENTES E EQUIPAMENTOS PARA LABORATORIOS LTDA. The registration is held by DOLES REAGENTES E EQUIPAMENTOS PARA LABORATORIOS LTDA 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 GOLD ANALISA DIAGNOSTICA LTDA, KATAL BIOTECNOLOGICA INDÚSTRIA E COMÉRCIO LTDA, 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
10231810020
Registration Details
ANVISA Registration Number: 10231810020
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

CREATINA FOSFOTRANSFERASE (CPK)
Risk Class II

Registration Details

10231810020

2500506528596

01085513000105

Company Information

Dates and Status

Dec 19, 1996

VIGENTE

09/18/2025 19:00:01