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sthemA FD-50

EUDAMED

Class A (EU MDR)

Ref 01471Model sthemA FD-50

by Tcoag ireland ltd

Identity

Trade Name
sthemA FD-50 EUDAMED
Device Name
sthemA FD-50 EUDAMED
Model / Reference
sthemA FD-50 EUDAMED
01471 EUDAMED

Identifiers

Primary DI / UDI-DI
05391521421982 EUDAMED
Basic UDI-DI
53915214FD50HR EUDAMED
Direct Marketing DI
05391521421982 EUDAMED
EMDN Code
W0103010105 CBC-REAGENTS (CLEANING-/DILUTING-/LYSING-/SHEATH-FLUIDS) 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

sthemA FD-50 by Tcoag ireland ltd — 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
Tcoag ireland ltd
EUDAMED SRN
IE-MF-000027371

Sources (1)

  • EUDAMED 8b422c9e-dc83-4771-9f52-5790d8aeaa31 61 fields · synced Jun 20, 2026