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LENTELL Fistula Touch XL

EUDAMED

Class I (EU MDR)

Ref 201151

by Lentismed d.o.o.

Identity

Trade Name
LENTELL Fistula Touch XL EUDAMED
Device Name
Ostomy Products EUDAMED
Model / Reference
201151 EUDAMED

Identifiers

Primary DI / UDI-DI
03858892216637 EUDAMED
Basic UDI-DI
385889221stomaprodsSF EUDAMED
EMDN Code
A100199 DEVICES FOR ABDOMINAL OSTOMY - ONE PIECE - OTHER 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

Category: One-piece intestinal ostomy bag, closed-ended

LENTELL Fistula Touch XL by Lentismed d.o.o. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as One-piece intestinal ostomy bag, closed-ended.

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 cb28468b-e413-472a-9282-5705a2212166 61 fields · synced Jun 18, 2026