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Suction liner 2000ML (without shut-off filter, pre-loaded SAP)

by Yung Kang Medical Device Technology Co., Ltd. 5 variants

Ref SG2019

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number471987332YKSG001ZQ Basic UDI-DI 04719873323852UDI-DIDate19 Apr 2024RegisteredStatusActive

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  • Withdrawn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
Suction Liner
Model / Reference
SG2019
Primary DI / UDI-DI
04719873323852
Basic UDI-DI
471987332YKSG001ZQ
EMDN Code
A060301 Collection bags and other containers for drainages and fistulas, single use
Device Class
Class I
EU market of registration
Romania

Manufacturer details

EUDAMED SRN
TW-MF-000028843
Authorised representative
Lotus NL B.V. NL-AR-000000121

Other devices from Yung Kang Medical Device Technology Co., Ltd.

See all devices from Yung Kang Medical Device Technology 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