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Adrenocorticotropic Hormone (ACTH) Assay Reagent Kit (CMIA)

EUDAMED

Class IVD General (EU MDR)

Ref C2KJ002

by Hangzhou Cybereagen Biotech Co., Ltd.

Identity

Trade Name
Adrenocorticotropic Hormone (ACTH) Assay Reagent Kit (CMIA) EUDAMED
Model / Reference
C2KJ002 EUDAMED

Identifiers

Primary DI / UDI-DI
06976753471210 EUDAMED
Basic UDI-DI
B-06976753471210 EUDAMED
EMDN Code
W0102060401 ADRENOCORTICOTROPIC HORMONE 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

Adrenocorticotropic Hormone (ACTH) Assay Reagent Kit (CMIA) by Hangzhou Cybereagen Biotech Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED

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 8478d3ea-30c6-4220-9bef-664132075e18 61 fields · synced Oct 7, 2026