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Lentell IleoTouch L75

EUDAMED

Class I (EU MDR)

Ref 201173F

by Lentismed d.o.o.

Identity

Trade Name
Lentell IleoTouch L75 EUDAMED
Device Name
Ostomy Products EUDAMED
Model / Reference
201173F EUDAMED

Identifiers

Primary DI / UDI-DI
03858892219621 EUDAMED
Basic UDI-DI
385889221stomaprodsSF EUDAMED
EMDN Code
A1001020102 ONE-PIECE ILEOSTOMY BAGS FOR NON-RETRACTED STOMA, FLAT, WITH TISSUE COVER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Croatia EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Lentell IleoTouch L75 by Lentismed d.o.o. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Lentismed d.o.o.
EUDAMED SRN
HR-MF-000018298

Sources (1)

  • EUDAMED 6de002d7-03d1-4c72-bff1-3f960e698fd1 61 fields · synced Jun 18, 2026