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Lem

by SAPI MED S.p.A. EUDAMED

Active European Union

Ref A.5660.5LFDModel Ligator

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number803363880BNDLGTRKG Basic UDI-DIDate13 Mar 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Ligator
Model / Reference
Ligator, A.5660.5LFD
Primary DI / UDI-DI
08033638803653
Basic UDI-DI
803363880BNDLGTRKG, 803363880LEMTRAZKITKX
EMDN Code
G020401 Haemorrhoid ligature sets
Device Class
Class I
Market of Registration
Italy
Medical Purpose
Legatura emorroidi

Manufacturer details

EUDAMED SRN
IT-MF-000023733

Other devices from SAPI MED S.p.A.

See all devices from SAPI MED S.p.A. →

Properties

Show properties
Other properties (13)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No