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Proctology Kit

by Ceram Optec SIA 41 variants

Ref 501400520-1

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number404908964PD Basic UDI-DI 04049089106551UDI-DIDate14 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  • Withdrawn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
501400520-1
Primary DI / UDI-DI
04049089106551
Basic UDI-DI
404908964PD
EMDN Code
Z12011085 Laser surgery instruments - consumables
Device Class
Class IIa
Medical Purpose
Procedure pack intended for proctological procedures utilizing photothermolytic effects on tissue to treat diseases according to the indications.

Manufacturer details

EUDAMED SRN
LV-PR-000053390

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See all devices from Ceram Optec SIA →

Properties

Other properties (1)

  • Sterile: No