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Proctology Kit

by CeramOptec GmbH 41 variants

Ref 502400510-3

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number404905964NQ Basic UDI-DI 04049059580923UDI-DIDate16 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  • Withdrawn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
Proctology Kit
Model / Reference
502400510-3
Primary DI / UDI-DI
04049059580923
Basic UDI-DI
404905964NQ
EMDN Code
Z12011085 Laser surgery instruments - consumables
Device Class
Class IIa
Medical Purpose
The product group Proctology consists of flexible fiberoptic cables that serve to deliver laser light to treat patients during proctological procedures. The fibers are used with or without an appropriate endoscope (proctoscope) for procedures utilizing photothermolytic effects on tissue to treat diseases according to the indications.

Manufacturer details

EUDAMED SRN
DE-PR-000052739

Other devices from CeramOptec GmbH

See all devices from CeramOptec GmbH →

Properties

Other properties (1)

  • Sterile: No