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Gaoton

by Xi’an Surgical Medical Technology Co., Ltd. 32 variants

Ref DQG-E3830-A250Model DQG-E4645-A130

Active European Union

CE MDD

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06927263610606 Basic UDI-DI Date21 Oct 2026RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
Sterile Bipolar HF Plasma Electrodes
Model / Reference
DQG-E3830-A250, DQG-E4645-A130
Primary DI / UDI-DI
06927263610606, 06927263614925, 06927263614918
Basic UDI-DI
B-06927263610606, B-06927263614925, B-06927263614918
EMDN Code
K02010199 Mono- and bipolar instruments, single-use - other
Device Class
Class IIb
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000026895
Authorised representative
Luxus Lebenswelt GmbH DE-AR-000005110

Other devices from Xi’an Surgical Medical Technology Co., Ltd.

See all devices from Xi’an Surgical Medical Technology Co., Ltd. →

Properties

  • Sterile

Other properties (10)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No