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Sheath

EUDAMED

Class A (EU MDR)

Ref 3020855

by Dirui Industrial Co., Ltd

Identity

Trade Name
Sheath EUDAMED
Device Name
Urinalysis Reagent EUDAMED
Model / Reference
3020855 EUDAMED

Identifiers

Primary DI / UDI-DI
06925794587480 EUDAMED
Basic UDI-DI
69257945W010106020302R0FD EUDAMED
EMDN Code
W010106020302 URINE SEDIMENT TEST KIT (AUTOMATED) EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Belgium 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

Sheath by Dirui Industrial 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-000001891
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED 73424044-6caf-4918-b78b-f4865c76a90c 61 fields · synced Jun 18, 2026