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LENTELL IleoBag II S; transparent; flexi

by Lentismed d.o.o. Croatia EUDAMED

Ref 201110-1F

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
201110-1F
Primary DI / UDI-DI
03858892215548
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 785179df-2ef4-4fd0-829a-89d9467c66c8 61 fields · synced 22 Oct 2026