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geko

EUDAMED

Class IIa (EU MDR)

Ref T3RWP2-03Model T-3 pack

by Firstkind Limited

Identity

Trade Name
geko EUDAMED
Device Name
Neuromuscular Stimulation Device Pack EUDAMED
Model / Reference
T-3 pack EUDAMED
T3RWP2-03 EUDAMED

Identifiers

Primary DI / UDI-DI
05060294772026 EUDAMED
Basic UDI-DI
506029477T3pkEC EUDAMED
EMDN Code
N0199 ENCEPHALIC AND PERIPHERAL NERVOUS SYSTEM DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Medical Purpose
• to increase blood circulation • for the prevention of venous thrombosis • for the prevention and treatment of oedema EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

geko by Firstkind Limited — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Firstkind Limited
EUDAMED SRN
UK-PR-000040065

Sources (1)

  • EUDAMED ee5094bb-d7cf-4ec8-91f0-f7cf6e7432cd 61 fields · synced May 23, 2026