Identity
- Trade Name
- LENTELL OstoPowder EUDAMED
- Device Name
- Ostomy Accessories EUDAMED
- Model / Reference
- 201129 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03858892215012 EUDAMED
- Basic UDI-DI
- 385889221stomaaccssHJ EUDAMED
- EMDN Code
- A108003 PROTECTIVE POWDERS 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 OstoPowder 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 385889221stomaaccssHJ | Class I | Active |
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Manufacturer
- Manufacturer
- Lentismed d.o.o.
- EUDAMED SRN
- HR-MF-000018298
Sources (1)
- EUDAMED 15692905-4c42-4760-9261-d4321c5ece72 61 fields · synced Jun 19, 2026