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Omlipo ASO Kit

EUDAMED

Class IVD General (EU MDR)

Ref OP21050Ref OP21100

by Goldsite Diagnostics Inc.

Identity

Trade Name
Omlipo ASO Kit EUDAMED
Device Name
Omlipo ASO Kit EUDAMED
Model / Reference
OP21050 EUDAMED
OP21100 EUDAMED

Identifiers

Primary DI / UDI-DI
06971225930660 EUDAMED
06971225939625 EUDAMED
Basic UDI-DI
B-06971225930660 EUDAMED
B-06971225939625 EUDAMED
EMDN Code
W01021104 ANTI-STREPTOLYSIN O (QUANTITATIVE) 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 ASO 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 cb922f1b-a612-4cf3-9683-7bbbb443a9db 61 fields · synced Jul 28, 2026
  • EUDAMED 064055b2-0acf-4a0b-95f7-74dd6837502f 61 fields · synced May 18, 2026