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sthemO V

EUDAMED

Class B (EU MDR)

Ref 01230

by Diagnostica Stago

Identity

Trade Name
sthemO V EUDAMED
Device Name
sthemO V EUDAMED
Model / Reference
01230 EUDAMED

Identifiers

Primary DI / UDI-DI
13607450012306 EUDAMED
Basic UDI-DI
3607450FACT0018DQ EUDAMED
Unit of Use DI
03607450012309 EUDAMED
EMDN Code
W0103020204 COAGULATION FACTOR V EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

EUDAMED

Animal Tissues

Yes

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

sthemO V by Diagnostica Stago — Class B — 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 20f58682-0640-4aa1-9b67-85b5fa22c932 61 fields · synced Jun 19, 2026