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sthemO dRVV confirm

EUDAMED

Class B (EU MDR)

Ref 01239

by Diagnostica Stago

Identity

Trade Name
sthemO dRVV confirm EUDAMED
Device Name
sthemO dRVV confirm EUDAMED
Model / Reference
01239 EUDAMED

Identifiers

Primary DI / UDI-DI
13607450012399 EUDAMED
Basic UDI-DI
360745099LA0005XM EUDAMED
Unit of Use DI
03607450012392 EUDAMED
EMDN Code
W0103020606 LUPUS ANTICOAGULANT EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

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 dRVV confirm 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 d876dc70-4671-4d84-9112-d542d9a85c6e 61 fields · synced Jun 18, 2026