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Bare Fiber, single-use, sterile

by CeramOptec GmbH 60 variants

Part of a family of 89 devices: see the family page

Ref 503500502

Bare Fiber, single-use, sterile (503500502) is a Class IIa device made by CeramOptec GmbH, registered in EUDAMED on 1 Dec 2025 (Basic UDI-DI 404905902N2), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number404905902N2 Basic UDI-DI 04049059518261UDI-DIDate1 Dec 2025RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Bare Fiber, single-use, sterile
Model / reference
503500502
Primary DI / UDI-DI
04049059518261
Basic UDI-DI
404905902N2
EMDN code
Z12011085 Laser surgery instruments - consumables
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005607

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Category: Varicose vein lasing procedure kit

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Properties

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