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- Date of registration
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EUDAMED last updated this device on Oct 23, 2025
5709817D02P067S01206QDansac is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Dansac A/S. Placed on the EU market in Denmark. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
057098176048325709817D02P067S01206Q1321-70S(01)05709817604832
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
A10020202COLOSTOMY BAGS FOR TWO-PART SYSTEMS, WITH TISSUE COVERNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Denmark; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| DenmarkPrimary placement | Still on market |
DK-MF-000001514No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.