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URIT 5D 11 Diluent

EUDAMED

Class A (EU MDR)

Ref /Model URIT D31、URIT 5D 11

by URIT Medical Electronic Co., Ltd.

Identity

Trade Name
URIT 5D 11 Diluent EUDAMED
Device Name
Diluent EUDAMED
Model / Reference
URIT D31、URIT 5D 11 EUDAMED
/ EUDAMED

Identifiers

Primary DI / UDI-DI
06935740723114 EUDAMED
06935740723107 EUDAMED
06935740703116 EUDAMED
Basic UDI-DI
69357407IBHS000005E6 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 5D 11 Diluent by URIT Medical Electronic 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-000011840
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (3)

  • EUDAMED 22a0a767-96d7-4f51-affd-383c9a05755b 61 fields · synced Oct 6, 2026
  • EUDAMED ebce0883-d5e6-4b23-8c23-a1eb774a838e 61 fields · synced May 19, 2026
  • EUDAMED 481a361c-a0d4-4af1-bd58-b280589a59f3 61 fields · synced May 19, 2026