ANVISA registration 80254180485Valid until Dec 22, 2035CREATINE KINASE ISOENZYMES (CKMB, CKBB, CKMM)
ANVISA Registration Number: 80254180485PHADIA DIAGNOSTICOS LTDATHERMO FISHER SCIENTIFIC OYRisk Class III
Device names
- Technical name
- CREATINE KINASE ISOENZYMES (CKMB, CKBB, CKMM)
- Risk class
- Class III
PT: CREATINOQUINASE ISOENZIMAS (CKMB, CKBB, CKMM)
Registration details
- Registration Number
- 80254180485
- Process Number
- 25351179425202558
- CNPJ
- 04930429000139
Company information
- Registration Holder
- PHADIA DIAGNOSTICOS LTDA
- Manufacturer
- THERMO FISHER SCIENTIFIC OY
- Manufacturing Country
- Finland
PT: FINLÂNDIA
Dates and status
- Publication Date
- Dec 22, 2025
- Validity
- 22/12/2035
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for CREATINE KINASE ISOENZYMES (CKMB, CKBB, CKMM) in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80254180485 and manufactured by THERMO FISHER SCIENTIFIC OY. The registration is held by PHADIA DIAGNOSTICOS LTDA with validity until Dec 22, 2035.
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