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ELVeS® Kit

by CeramOptec GmbH 103 variants

Ref 503100158-5

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 Number404905961NJ Basic UDI-DI 04049059580503UDI-DIDate10 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  • Withdrawn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
ELVeS® Kit
Model / Reference
503100158-5
Primary DI / UDI-DI
04049059580503
Basic UDI-DI
404905961NJ
EMDN Code
Z12011085 Laser surgery instruments - consumables
Device Class
Class IIa
Medical Purpose
The ELVeS® Fibers are fiber optic cables for the treatment of varicose veins by photothermolysis, leading to the sealing of the treated vein with laser during surgical procedures.

Manufacturer details

EUDAMED SRN
DE-PR-000052739

Other devices from CeramOptec GmbH

See all devices from CeramOptec GmbH →

Properties

Other properties (1)

  • Sterile: No