← Back to catalogue

URIT 5L 31 Lyse

EUDAMED

Class A (EU MDR)

Ref /Model URIT 5L 31

by URIT Medical Electronic Co., Ltd.

Identity

Trade Name
URIT 5L 31 Lyse EUDAMED
Device Name
Lyse EUDAMED
Model / Reference
URIT 5L 31 EUDAMED
/ EUDAMED

Identifiers

Primary DI / UDI-DI
06935740741859 EUDAMED
Basic UDI-DI
69357407IBHS000033EB EUDAMED
EMDN Code
W0103010105 CBC-REAGENTS (CLEANING-/DILUTING-/LYSING-/SHEATH-FLUIDS) EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany 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

URIT 5L 31 Lyse by URIT Medical Electronic Co., Ltd. — Class A — CE/MDR — listed in EUDAMED — regulatory data on deviCERTS

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-000011840
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 9b4fa3af-c128-469e-9e16-4cb16c9a9deb 61 fields · synced Oct 7, 2026