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SPOTCHEM II Uric Acid

EUDAMED

Class IVD General (EU MDR)

Ref 77396Ref 77161

by ARKRAY Factory, Inc.

Identity

Trade Name
SPOTCHEM II Uric Acid EUDAMED
Device Name
SPOTCHEM II Uric Acid EUDAMED
Model / Reference
77396 EUDAMED
77161 EUDAMED

Identifiers

Primary DI / UDI-DI
D-77396K2 EUDAMED
D-77161J5 EUDAMED
Basic UDI-DI
B-77396K2 EUDAMED
B-77161J5 EUDAMED
EMDN Code
W01010232 URIC ACID EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Italy EUDAMED
Finland 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

Category: Uric acid IVD, reagent

SPOTCHEM II Uric Acid by ARKRAY Factory, Inc. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Uric acid IVD, reagent.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
JP-MF-000003008
Authorised Representative
ARKRAY Europe, B.V. NL-AR-000002056

Sources (2)

  • EUDAMED fbdffff5-6e22-4350-8a59-00b2aabb9370 61 fields · synced Jun 20, 2026
  • EUDAMED bd5d182d-7711-49bc-b991-7b0d7fb51aad 61 fields · synced Jun 20, 2026