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Lentell OstoProtect

EUDAMED

Class I (EU MDR)

Ref 201130L

by Lentismed d.o.o.

Identity

Trade Name
Lentell OstoProtect EUDAMED
Device Name
Ostomy Accessories EUDAMED
Model / Reference
201130L EUDAMED

Identifiers

Primary DI / UDI-DI
03858892219768 EUDAMED
Basic UDI-DI
385889221stomaaccssHJ EUDAMED
EMDN Code
A108004 PROTECTIVE FILMS / SPRAYS FOR PERISTOMAL SKIN 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 OstoProtect 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 1db91057-22b4-46dd-8e47-cf40f3dcf3c1 61 fields · synced Jun 19, 2026