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Lentell Flexi II S extended wear time

EUDAMED

Class I (EU MDR)

Ref 201119ET

by Lentismed d.o.o.

Identity

Trade Name
Lentell Flexi II S extended wear time EUDAMED
Device Name
Ostomy Products EUDAMED
Model / Reference
201119ET EUDAMED

Identifiers

Primary DI / UDI-DI
03858892219164 EUDAMED
Basic UDI-DI
385889221stomaprodsSF EUDAMED
EMDN Code
A1002010401 UNIVERSAL PLATES FOR ABDOMINAL STOMA (COLO-, ILEO-, UROSTOMY) WITH NON-INTROFLEX STOMA 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 Flexi II S extended wear time 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 e2ba4387-4ff8-4365-bba2-71da0561b26a 61 fields · synced Jul 23, 2026