Skip to content

Cobra

by A.R.C. Laser GmbH

Ref LS09011-DS, LS09011-LSModel LS09011

Cobra (LS09011-DS) is a medical device (EU MDR Class IIb; EMDN category multi–platform laser) made by A.R.C. Laser GmbH, registered in EUDAMED on 11 Jan 2024 (Basic UDI-DI 426015559COBRA4T), 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 Number426015559COBRA4T Basic UDI-DI Date11 Jan 2024RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
LS09011, LS09011-DS, LS09011-LS
Primary DI / UDI-DI
04260155593345, 04260155590009
Basic UDI-DI
426015559COBRA4T
Direct marketing DI
04260155593345
04260155590009
EMDN code
Z12011019 Multi–platform laser
Device class
Class IIb
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 MULTI–PLATFORM LASER.

Other devices from A.R.C. Laser GmbH

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

Properties

Other properties (14, all answered No)