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PercuFib

by LISA Laser Products GmbH

Ref 101 503 128, 101 503 665

Active European Union

CE MDD

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-04250341910605 Basic UDI-DI Date18 Feb 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Trade Name
PercuFib
PercuFib smart connector
Model / Reference
101 503 128, 101 503 665
Primary DI / UDI-DI
04250341910605, 04250341912050
Basic UDI-DI
B-04250341910605, B-04250341912050
EMDN Code
Z12011080 Laser surgery instruments - hardware accessories
Device Class
Class IIb
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005036

Other devices from Lisa Laser Products GmbH

See all devices from Lisa Laser Products GmbH →

Properties

  • Sterile NoEUDAMEDYesEUDAMED
  • Reusable YesEUDAMEDNoEUDAMED

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No