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ELVeS®

by Ceram Optec SIA 13 variants

Part of a family of 14 devices: see the family page

Ref 503300300

ELVeS® (503300300) is a Class IIa device made by Ceram Optec SIA, registered in EUDAMED on 14 May 2026 (Basic UDI-DI 404908901NM), active as of 22 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number404908901NM Basic UDI-DI 04049089003737UDI-DIDate14 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
ELVeS®
Model / reference
503300300
Primary DI / UDI-DI
04049089003737
Basic UDI-DI
404908901NM
EMDN code
Z12011085 Laser surgery instruments - consumables
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Latvia

Manufacturer details

EUDAMED SRN
LV-MF-000021846

Similar devices in this category

Other devices filed under LASER SURGERY INSTRUMENTS - CONSUMABLES.

Other devices from Ceram Optec SIA

See all devices from Ceram Optec SIA →

Properties

  • Supplied sterile
Other properties (13, all answered No)