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Taktvoll

by Beijing Taktvoll Technology Co., Ltd. 3 variants

Ref ES-120LEEP

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-06972960400043 Basic UDI-DI 06972960400043UDI-DIDate11 Mar 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  • Withdrawn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
High Frequency Surgical Generator
Model / Reference
ES-120LEEP
Primary DI / UDI-DI
06972960400043
Basic UDI-DI
B-06972960400043
EMDN Code
Z12010905 Radiosurgical units
Device Class
Class IIb
EU market of registration
Northern Ireland

Manufacturer details

EUDAMED SRN
CN-MF-000033674
Authorised representative
MedPath GmbH DE-AR-000000087

Other devices from Beijing Taktvoll Technology Co., Ltd.

See all devices from Beijing Taktvoll Technology Co., Ltd. →

Properties

Other properties (11)

  • Sterile: No
  • 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