Skip to content

ENFit Low Dose Enteral Syringe

by Medicina Limited EUDAMED

Active European Union

Ref LPE01LD

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05060278508900 Basic UDI-DIDate7 Jan 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
ENFit 1ml Low Dose Syringe
Model / Reference
LPE01LD
Primary DI / UDI-DI
05060278508900
Basic UDI-DI
B-05060278508900
EMDN Code
A020199 Syringes, single-use - other
Device Class
Class IIa
Market of Registration
Austria

Manufacturer details

EUDAMED SRN
UK-MF-000041402
Authorised representative
HMC PREMEDICAL S.P.A. IT-AR-000029439

Other devices from Medicina Limited

See all devices from Medicina Limited →

Properties

  • Sterile
  • Administering Medicine
  • Measuring Function

Other properties (8)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Incorporates Medicinal Product: No