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Medical compression knee stockings

by Tonus Elast Sia 18 variants

Ref 5621 Compressana Grace AD

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4750283JZKS1ZT Basic UDI-DI Date20 May 2025RegisteredStatusActive

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  • Withdrawn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
Medical compression products
Model / Reference
5621 Compressana Grace AD
Primary DI / UDI-DI
04067015929234, 04067015929098, 04067015929180, 04067015929296, 04067015929081, 04067015928916, 04067015929203, 04067015929302, 04067015929326, 04067015928886, 04067015929029, 04067015929074, 04067015928978, 04067015929067, 04067015929371, 04067015929173
Basic UDI-DI
4750283JZKS1ZT
EMDN Code
M030405 Compression stockings
Device Class
Class I
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
LV-MF-000006828

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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