Pure Global AI
ANVISA registration 10230730101Active

CREATINE KINASE (CK)

ANVISA Registration Number: 10230730101NL COMÉRCIO EXTERIOR LTDAHELENA LABORATORIESRisk Class II
Verified
Device names
Technical name
CREATINE KINASE (CK)
View exact technical-name matches →
PT: CREATINOQUINASE (CK)
Commercial name
Kit para Eletroforese SPIFE CK
View exact commercial-name matches →
Risk class
Class II
Registration details
Registration Number
10230730101
Process Number
25351004107201015
CNPJ
52541273000147
Company information
Registration Holder
NL COMÉRCIO EXTERIOR LTDA
Manufacturer
HELENA LABORATORIES
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
May 31, 2010
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

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 10230730101 and manufactured by HELENA LABORATORIES. The registration is held by NL COMÉRCIO EXTERIOR LTDA with validity until currently active (VIGENTE).

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.