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Anti-Mullerian Hormone Test (Up-converting Phosphor Technology)

EUDAMED

Class B (EU MDR)

Ref HGUPT15Model Please see the IFU

by Beijing Hotgen Biotech Co., Ltd.

Identity

Trade Name
Anti-Mullerian Hormone Test (Up-converting Phosphor Technology) EUDAMED
Device Name
Anti-Mullerian Hormone Test (Up-converting Phosphor Technology) EUDAMED
Model / Reference
Please see the IFU EUDAMED
HGUPT15 EUDAMED

Identifiers

Primary DI / UDI-DI
06936700403374 EUDAMED
Basic UDI-DI
697029753442LN EUDAMED
EMDN Code
W0102050215 ANTI-MULLERIAN HORMONE EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

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

New Device

No

EUDAMED

Anti-Mullerian Hormone Test (Up-converting Phosphor Technology) by Beijing Hotgen Biotech Co., Ltd. — Class B — IVDR — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000015566
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 17740266-ab43-48d1-9640-eabfaf3ef104 61 fields · synced Jun 18, 2026