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LightCut Plus

by M.D.L. S.r.l. 10 variants

Ref PD1607

LightCut Plus (PD1607) is a Class IIa device made by M.D.L. S.R.L., registered in EUDAMED on 3 Nov 2026 (Basic UDI-DI B-08055271577340), 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-08055271577340 Basic UDI-DI 08055271577340UDI-DIDate3 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
PD1607
Primary DI / UDI-DI
08055271577340
Basic UDI-DI
B-08055271577340
EMDN code
A0102010101 Shearing biopsy needles
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
IT-MF-000011599

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Properties

  • Supplied sterile
Other properties (11, all answered No)