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Alterna

by Coloplast A/S Denmark EUDAMED

Ref 17710

EMDN A1002010401

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number57089322976118P Basic UDI-DIDate27 Mar 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Alterna (Upgrade Original) ostomy baseplate
Model / Reference
17710
Primary DI / UDI-DI
05708932889841, 05708932634953, 05708932769112, 05708932081931
Basic UDI-DI
57089322976118P
Unit of Use DI
05708932887922, 05701780141857, 05708932769105, 05708932081924
EMDN Code
A1002010401 Universal plates for abdominal stoma (colo-, ileo-, urostomy) with non-introflex stoma
Device Class
Class I
Market of Registration
Spain
Hungary
Bulgaria
Romania

Manufacturer details

EUDAMED SRN
DK-MF-000025526

Other devices from Coloplast A/S

See all devices from Coloplast A/S →

Properties & raw data

Show properties, registry sources and raw records
Other properties (13)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (4)

  • EUDAMED 033f0422-1061-4a65-9070-9a21609b2263 61 fields · synced 22 Oct 2026
  • EUDAMED 05708932634953|57089322976118P 61 fields · synced 16 May 2026
  • EUDAMED 05708932769112|57089322976118P 61 fields · synced 18 May 2026
  • EUDAMED 05708932081931|57089322976118P 61 fields · synced 19 May 2026