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Cetus Probe

by A.R.C. Laser GmbH

Ref LY11004s

Cetus Probe (LY11004s) is a medical device (EU MDR Class IIa; EMDN category laser surgery instruments - consumables) made by A.R.C. Laser GmbH, registered in EUDAMED on 6 Nov 2026 (Basic UDI-DI 426015559CetusProbePC), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number426015559CetusProbePC Basic UDI-DI 04260155592447UDI-DIDate6 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
LY11004s
Primary DI / UDI-DI
04260155592447
Basic UDI-DI
426015559CetusProbePC
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-000009383

Similar devices in this category

Other devices filed under LASER SURGERY INSTRUMENTS - CONSUMABLES.

Other devices from A.R.C. Laser GmbH

See all devices from A.R.C. Laser GmbH →

Properties

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