Identity
- Trade Name
- Alterna EUDAMED
- Device Name
- Alterna (Upgrade New Generation) ostomy bag 1-piece closed EUDAMED
- Model / Reference
- 13514 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05708932528702 EUDAMED
- Basic UDI-DI
- 570893229752893 EUDAMED
- Unit of Use DI
- 05708932539968 EUDAMED
- EMDN Code
- A1001010102,A1001020102 EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Spain 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
Alterna by Coloplast A/S — 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 | 570893229752893 | Class I | Active |
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Manufacturer
- Manufacturer
- Coloplast A/S
- EUDAMED SRN
- DK-MF-000025526
Sources (1)
- EUDAMED 0f146866-9e77-4376-a1ad-8f4262558b9e 61 fields · synced May 29, 2026