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ActiLymph Hosiery Applicator

by Lohmann & Rauscher Medical UK Ltd

Ref 88320

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, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5037696ActiglideFV Basic UDI-DI 05037696400215UDI-DIDate11 Aug 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
ActiGlide Hosiery Applicator
Model / Reference
88320
Primary DI / UDI-DI
05037696400215
Basic UDI-DI
5037696ActiglideFV
EMDN Code
M030405 Compression stockings
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
UK-MF-000036885
Authorised representative
Lohmann & Rauscher International GmbH & Co. KG DE-AR-000005187

From the manufacturer

Manufacturer's product page: ActiLymph

Other devices from Lohmann & Rauscher Medical UK Ltd

See all devices from Lohmann & Rauscher Medical UK Ltd →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No