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CK-MB Rapid Test Device - Serum

EUDAMED

Class IVD General (EU MDR)

Ref J020501D

by Hangzhou Cybereagen Biotech Co., Ltd.

Identity

Trade Name
CK-MB Rapid Test Device (Whole Blood/Serum/Plasma) EUDAMED
Model / Reference
J020501D EUDAMED

Identifiers

Primary DI / UDI-DI
06976753474990 EUDAMED
Basic UDI-DI
B-06976753474990 EUDAMED
EMDN Code
W01021311 CREATINE KINASE - MB MASS (IC) EUDAMED
Models / Variants
Whole Blood EUDAMED
Serum EUDAMED
Plasma EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

CK-MB Rapid Test Device - Serum by Hangzhou Cybereagen Biotech Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED — 3 models

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000037850
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED ad0d941a-0778-4086-bfb8-dafbdc7331b2 61 fields · synced Oct 6, 2026