Skip to content

Winelec

by Wonjin Mulsan Co., Ltd. 5 variants

Ref CT-Q80B0Model POWER-Q8120/ POWER-Q8060/PREMIUM6

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 linked in EUDAMED

A group certificate may exist

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 Number880927742P800XF6 Basic UDI-DI Date23 Aug 2024RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Power-Q8120/ Power-Q8060/PREMIUM6
Model / Reference
POWER-Q8120/ POWER-Q8060/PREMIUM6, CT-Q80B0
Primary DI / UDI-DI
18809277423388, 08809277420182
Basic UDI-DI
880927742P800XF6
EMDN Code
Z120607 Pneumatic compression equipment
Device Class
Class IIa
EU market of registration
France

Manufacturer details

EUDAMED SRN
KR-MF-000001420
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Wonjin Mulsan Co.ltd

See all devices from Wonjin Mulsan 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