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ANVISA registration 80048490061Active

CREATINE KINASE (CK)

ANVISA Registration Number: 80048490061USA DIAGNOSTICA LTDAMONOBIND INCRisk Class II
Verified
Device names
Technical name
CREATINE KINASE (CK)
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PT: CREATINOQUINASE (CK)
Commercial name
CK-MB (CREATINE KINASE) TEST SYSTEM
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Risk class
Class II
Registration details
Registration Number
80048490061
Process Number
25351316198201037
CNPJ
02330159000108
Company information
Registration Holder
USA DIAGNOSTICA LTDA
Manufacturer
MONOBIND INC
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Feb 06, 2012
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 80048490061 and manufactured by MONOBIND INC. The registration is held by USA DIAGNOSTICA 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.