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Anti Embolism Stocking

by Zhejiang Chunde Medical Equipment Co., Ltd

Ref KXSQADSModel KXSQ(AD, AG),(S, M, L, XL), KXSPQ(AD, AG),(S, M, L, XL)

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 Number697879133AMS001RM Basic UDI-DI 06978791330108UDI-DIDate6 Mar 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  • Withdrawn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
Anti Embolism Stocking
Model / Reference
KXSQ(AD, AG), (S, M, L, XL), KXSPQ(AD, KXSQADS
Primary DI / UDI-DI
06978791330108
Basic UDI-DI
697879133AMS001RM
EMDN Code
M030499 Elastic bandages, support and compression - other
Device Class
Class I
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000051657
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Zhejiang Chunde Medical Equipment Co., 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