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ELVeS® Kit

by Ceram Optec SIA 103 variants

Ref 501100160-1

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 Number404908961P7 Basic UDI-DI 04049089106728UDI-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  • Withdrawn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
ELVeS® Kit
Model / Reference
501100160-1
Primary DI / UDI-DI
04049089106728
Basic UDI-DI
404908961P7
EMDN Code
Z12011085 Laser surgery instruments - consumables
Device Class
Class IIa
Medical Purpose
Procedure pack intended for endovenous laser treatment of varicose veins and endoluminal closure of venous insufficiencies.

Manufacturer details

EUDAMED SRN
LV-PR-000053390

Other devices from Ceram Optec SIA

See all devices from Ceram Optec SIA →

Properties

Other properties (1)

  • Sterile: No