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OWL GD-Pad Patient Return Electrode (Corded)

by Diros Technology Inc.

Ref D7506

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0825114DN7506AM Basic UDI-DI 00825114008427UDI-DIDate26 Jun 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
OWL GD-Pad Patient Return Electrode (Corded)
Model / Reference
D7506
Primary DI / UDI-DI
00825114008427
Basic UDI-DI
0825114DN7506AM
Direct Marketing DI
00825114008427
EMDN Code
K02010201 Electrosurgery single patient pads (neutral electrodes), single-use
Device Class
Class IIb
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CA-MF-000007423
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from Diros Technology, Inc.

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