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ENFit Enteral Syringe

by Medicina Limited United Kingdom EUDAMED

Ref LPE10 EMDN A020199

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05060278507439 Basic UDI-DIDate9 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  • Withdrawn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 · synced 24 Oct 2026

Device Name
10ml ENFit Enteral Syringe
Model / Reference
LPE10
Primary DI / UDI-DI
05060278507439
Basic UDI-DI
B-05060278507439
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 & raw data

Show properties, registry sources and raw records
  • 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

Sources (1)

  • EUDAMED 7b4e3b4e-dbf5-45e6-ba4b-8a2794eaa8db 61 fields · synced 24 Oct 2026