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Omlipo RF Kit

EUDAMED

Class IVD General (EU MDR)

Ref OP23100Ref OP23050

by Goldsite Diagnostics Inc.

Identity

Trade Name
Omlipo RF Kit EUDAMED
Device Name
Omlipo RF Kit EUDAMED
Model / Reference
OP23100 EUDAMED
OP23050 EUDAMED

Identifiers

Primary DI / UDI-DI
06971225930691 EUDAMED
06971225930684 EUDAMED
Basic UDI-DI
B-06971225930691 EUDAMED
B-06971225930684 EUDAMED
EMDN Code
W01021110 RHEUMATOID FACTORS EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Italy 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

Omlipo RF Kit by Goldsite Diagnostics Inc. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000001353
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (2)

  • EUDAMED 66b6936b-6892-4b8c-9d60-333e6d5537c8 61 fields · synced Jul 28, 2026
  • EUDAMED 40c36f8c-b581-4d17-975e-df833a399e8b 61 fields · synced May 17, 2026