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ElectrodeCRF

by Cambridge Interventional LLC 116 variants

Ref CRF-N2505-B

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-10811746030339 Basic UDI-DI 10811746030339UDI-DIDate22 Jul 2022RegisteredStatusActive

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  • Withdrawn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
Crf-N2505-B
Model / Reference
CRF-N2505-B
Primary DI / UDI-DI
10811746030339
Basic UDI-DI
B-10811746030339
EMDN Code
Z12010902 Electrosurgical units (esu) for general use
Device Class
Class IIb
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
US-MF-000021911
Authorised representative
MDSS GmbH DE-AR-000005430

Related devices

Category: Foot-switch, electrical

Other devices from Cambridge Interventional LLC

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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