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LENTELL ileobag II L; transparent

by Lentismed d.o.o. Croatia EUDAMED

Ref 201111-1

EMDN A10020301

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number385889221stomaprodsSF Basic UDI-DIDate22 Dec 2021RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Ostomy Products
Model / Reference
201111-1
Primary DI / UDI-DI
03858892214756
Basic UDI-DI
385889221stomaprodsSF
EMDN Code
A10020301 Ileostomy bags for two-part systems, w/o tissue cover
Device Class
Class I
Market of Registration
Croatia

Manufacturer details

EUDAMED SRN
HR-MF-000018298

Other devices from Lentismed d.o.o.

See all devices from Lentismed d.o.o. →

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED 9b135379-4487-4e0d-b0e1-4e2e27568481 61 fields · synced 22 Oct 2026