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GHgb-Lyse

EUDAMED

Class A (EU MDR)

Ref 60104Model Lyse-G

by B&E Bio-Technology Co., Ltd.

Identity

Trade Name
GHgb-Lyse EUDAMED
Device Name
GHgb-Lyse EUDAMED
Model / Reference
Lyse-G EUDAMED
60104 EUDAMED

Identifiers

Primary DI / UDI-DI
06972337851867 EUDAMED
Basic UDI-DI
697233785GHgbLyse009BZ EUDAMED
EMDN Code
W0103010299 OTHER HAEMOGLOBIN (TYPES) TESTING - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Austria 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

New Device

No

EUDAMED

GHgb-Lyse by B&E Bio-Technology Co., Ltd. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000023256
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED 51dd5867-1d23-4dc0-9c7e-d6f473ecf872 61 fields · synced Jul 12, 2026