Skip to content

Ace HF Loop/ Electrode- LEEP/ LLETZ Electrode, 1.2 cm W x 1.5 cm D, 13 cm Shaft

by Ace Medical Devices Pvt Ltd

Ref AR 121513Model HF Electrode (LEEP/LLETZ Electrode Variant) _AR 121513

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 7 Nov 2026. What this means

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08904148108241 Basic UDI-DI 08904148108241UDI-DIDate14 May 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  • Withdrawn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

Model / Reference
HF Electrode (LEEP/LLETZ Electrode Variant) _AR 121513, AR 121513
Primary DI / UDI-DI
08904148108241
Basic UDI-DI
B-08904148108241
EMDN Code
K0201010301 Open electrosurgery electrodes, single-use
Device Class
Class IIb
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
IN-MF-000023786
Authorised representative
Advena Limited MT-AR-000000234

Other devices from Ace Medical Devices Pvt Ltd

See all devices from Ace Medical Devices Pvt 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