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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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CK-MB — 2 UDI-DI variants, IVDR (Thermo Fisher Scientific Oy)

MD Atlas
Thermo Fisher Scientific Oy

Data from EUDAMED, last updated May 23, 2026

CK-MB

6438153BU00052BL

2 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class C

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Manufacturer: Thermo Fisher Scientific Oy

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 6438153BU00052BL
Device name: CK-MB
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Version date: Nov 29, 2023

Manufacturer & authorised representative

Manufacturer

Name: Thermo Fisher Scientific Oy
SRN: FI-MF-000001479
Country: Finland
Email: registrations.clinical.fi@thermofisher.com
Phone: +358 10 329 200

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HGDDW3NNN3EECF7MBENPG5KJ

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

CK-MB16438153818370
CK-MB16438153818349