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Disposable Saliva Ejectors

by Changzhou Youkerui Technology Development Co., Ltd 8 variants

Ref XTG-AModel XTG-A, XTG-B-1, XTG-B-2, XTG-C-1, XTG-C-2, XTG-C-3, XTG-D, XTG-E

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 Number698053585YKR-DSE7B Basic UDI-DIDate14 Sep 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No notified-body 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  • Withdrawn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

Model / Reference
XTG-A, XTG-B-1, XTG-B-2, XTG-C-1, XTG-C-2, XTG-C-3, XTG-D, XTG-E
Primary DI / UDI-DI
06980535850018
Basic UDI-DI
698053585YKR-DSE7B
EMDN Code
Q019001 Saliva aspirators and saliva absorbents
Device Class
Class I
Market of Registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000058732
Authorised representative
HyperCert Limited B.V. NL-AR-000047746

Other devices from Changzhou Youkerui Technology Development Co., Ltd

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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