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Altiform

by urgo ltd United Kingdom EUDAMED

Ref 558009Model 558009 511KO12 EMDN M030405

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-5060064271117R2 Basic UDI-DIDate11 Feb 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
AltiForm Below knee class I small open toe beige
Model / Reference
558009 511KO12, 558009
Primary DI / UDI-DI
D-5060064271117R2
Basic UDI-DI
B-5060064271117R2
EMDN Code
M030405 Compression stockings
Device Class
Class I
Market of Registration
Ireland

Manufacturer details

EUDAMED SRN
GB-MF-000029696
Authorised representative
LABORATOIRES URGO FR-AR-000022224

Other devices from urgo ltd

See all devices from urgo ltd →

Properties & raw data

Show properties, registry sources and raw records
Other properties (11)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED d32d20b0-5350-4576-aa52-2fc02bb39bb7 61 fields · synced 22 Oct 2026