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Luteinizing Hormone test (Up-converting Phosphor Technology)

EUDAMED

Class B (EU MDR)

Ref HGUPT33Model Please see the IFU

by Beijing Hotgen Biotech Co., Ltd.

Identity

Trade Name
Luteinizing Hormone test (Up-converting Phosphor Technology) EUDAMED
Device Name
Luteinizing Hormone test (Up-converting Phosphor Technology) EUDAMED
Model / Reference
Please see the IFU EUDAMED
HGUPT33 EUDAMED

Identifiers

Primary DI / UDI-DI
06936700410051 EUDAMED
Basic UDI-DI
6970297531057AN EUDAMED
EMDN Code
W0102050105 LUTEINISING 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

Luteinizing 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 822f87c3-8fca-411b-8088-992cd0484556 61 fields · synced Jun 18, 2026