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LENTELL OstoZip II M

EUDAMED

Class I (EU MDR)

Ref 201168

by Lentismed d.o.o.

Identity

Trade Name
LENTELL OstoZip II M EUDAMED
Device Name
Ostomy Products EUDAMED
Model / Reference
201168 EUDAMED

Identifiers

Primary DI / UDI-DI
03858892217344 EUDAMED
Basic UDI-DI
385889221stomaprodsSF EUDAMED
EMDN Code
A100205 EXPANSION CAPS FOR TWO-PIECE ABDOMINAL OSTOMY SYSTEMS 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 OstoZip II M 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 338d6349-0f29-4dc5-8d2c-8b7c9af361cf 61 fields · synced Jul 11, 2026