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Glycosylated hemoglobin test (Up-converting Phosphor Technology)

EUDAMED

Class C (EU MDR)

Ref HGUPT22Model Please see the IFU

by Beijing Hotgen Biotech Co., Ltd.

Identity

Trade Name
Glycosylated hemoglobin test (Up-converting Phosphor Technology) EUDAMED
Device Name
Glycosylated hemoglobin test (Up-converting Phosphor Technology) EUDAMED
Model / Reference
Please see the IFU EUDAMED
HGUPT22 EUDAMED

Identifiers

Primary DI / UDI-DI
06936700408768 EUDAMED
Basic UDI-DI
697029753438LX EUDAMED
EMDN Code
W0102060109 GLYCOSYLATED/GLYCATED HAEMOGLOBIN (IC) EUDAMED

Classification

Device Class
Class C 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

Glycosylated hemoglobin test (Up-converting Phosphor Technology) by Beijing Hotgen Biotech Co., Ltd. — Class C — IVDR — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

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

Sources (1)

  • EUDAMED 69cd20d1-79be-4500-9ca8-98b70e004c05 61 fields · synced Jun 19, 2026