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LENTELL IleoTouch L

EUDAMED

Class I (EU MDR)

Ref 201108ET

by Lentismed d.o.o.

Identity

Trade Name
LENTELL IleoTouch L EUDAMED
Device Name
Ostomy Products EUDAMED
Model / Reference
201108ET EUDAMED

Identifiers

Primary DI / UDI-DI
03858892220009 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 L 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 ccc63c67-65e5-4f5a-add6-89d3f4c63020 61 fields · synced Jun 19, 2026