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Thrombocare

by Arden Medical 3 variants

Ref 9521-XL, 9521-XXL, 9511-XL, 9521-M, 9521-XS, 9521-L, 9511-MModel 9511-S

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number86805429Y0612MM Basic UDI-DI Date18 Feb 2026RegisteredStatusActive EUDAMED: not on the EU market

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  • Withdrawn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
Anti-Embolism Stockings-Calf
Model / Reference
9511-S, 9521-XL, 9521-XXL, 9511-XL, 9521-M, 9521-XS, 9521-L, 9511-M
Primary DI / UDI-DI
08680542902752, 08680542902769, 08680542902806, 08680542902738, 08680542902776, 08680542905241, 08680542902745, 08680542902783
Basic UDI-DI
86805429Y0612MM
EMDN Code
M030405 Compression stockings
Device Class
Class I

Manufacturer details

EUDAMED SRN
TR-MF-000026387

Other devices from Arden Medical

See all devices from Arden Medical →

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