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by Firstkind Limited 12 variants

Ref W3FE01-07Model W-3 pack

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number506029477W3pkEZ Basic UDI-DI Date21 Mar 2024RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Neuromuscular Stimulation Device Pack
Model / Reference
W-3 pack, W3FE01-07
Primary DI / UDI-DI
05060294772118, 05060294771555
Basic UDI-DI
506029477W3pkEZ
EMDN Code
N0199 Encephalic and peripheral nervous system devices - other
Device Class
Class IIa
Medical Purpose
• to increase blood circulation • for the treatment of oedema • for promoting wound healing • for the treatment of venous insufficiency and ischemia

Manufacturer details

EUDAMED SRN
UK-PR-000040065

Other devices from Firstkind, Ltd.

See all devices from Firstkind, Ltd. →

Properties

Other properties (1)

  • Sterile: No