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Adrenocor Ticotropic Hormore(ACTH)Assay Kit

EUDAMED

Class IVD General (EU MDR)

Ref 69543760F000656MModel 100 Tests

by Beijing Leadman Biochemistry Co., Ltd.

Identity

Trade Name
Adrenocor Ticotropic Hormore(ACTH)Assay Kit EUDAMED
Device Name
Adrenocor Ticotropic Hormore(ACTH)Assay Kit EUDAMED
Model / Reference
100 Tests EUDAMED
69543760F000656M EUDAMED

Identifiers

Primary DI / UDI-DI
06954376005470 EUDAMED
Basic UDI-DI
B-06954376005470 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

Yes

EUDAMED

Microbial Substances

Yes

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

Adrenocor Ticotropic Hormore(ACTH)Assay Kit by Beijing Leadman Biochemistry 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-000020150
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED ef51fcee-5342-4d1a-af52-28fc7cc50fa6 61 fields · synced Oct 6, 2026