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sthemO CK Prest

EUDAMED

Class C (EU MDR)

Ref 01223

by Diagnostica Stago

Identity

Trade Name
sthemO CK Prest EUDAMED
Device Name
sthemO CK Prest EUDAMED
Model / Reference
01223 EUDAMED

Identifiers

Primary DI / UDI-DI
03607450012231 EUDAMED
Basic UDI-DI
3607450APTT0006RE EUDAMED
EMDN Code
W0103020102 ACTIVATED PARTIAL THROMBOPLASTIN TIME EUDAMED

Classification

Device Class
Class C EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

Yes

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

sthemO CK Prest by Diagnostica Stago — Class C — 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

Manufacturer
Diagnostica Stago
EUDAMED SRN
FR-MF-000017089

Sources (1)

  • EUDAMED 490b5720-00e4-49a6-b530-cd440cbb0b4e 61 fields · synced Jul 10, 2026