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MultiPulse PRO 40

by Asclepion Laser Technologies GmbH

Ref J18-3100-000

MultiPulse PRO 40 (J18-3100-000) is a Class IIb device made by Asclepion Laser Technologies GmbH, registered in EUDAMED on 10 Aug 2026 (Basic UDI-DI B-04058784001047), active as of 7 Nov 2026.

Active European Union

CE MDD

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/MDD NumberB-04058784001047 Basic UDI-DI 04058784001047UDI-DIDate10 Aug 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
J18-3100-000
Primary DI / UDI-DI
04058784001047
Basic UDI-DI
B-04058784001047
EMDN code
Z12011005 Carbon dioxide surgical laser
Device class
Class IIb
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005158

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Properties

Other properties (12, all answered No)