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sthemO Desorb

EUDAMED

Class A (EU MDR)

Ref 01263

by Diagnostica Stago

Identity

Trade Name
sthemO Desorb EUDAMED
Device Name
sthemO Desorb EUDAMED
Model / Reference
01263 EUDAMED

Identifiers

Primary DI / UDI-DI
13607450012634 EUDAMED
Basic UDI-DI
3607450AUXI0014RV EUDAMED
Unit of Use DI
03607450012637 EUDAMED
EMDN Code
W0103020999 AUXILIARY REAGENTS (HAEMOSTASIS) - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
France 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

New Device

No

EUDAMED

sthemO Desorb by Diagnostica Stago — Class A — 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 b4453911-c5f7-4443-9674-b27e486d5270 61 fields · synced Jul 17, 2026