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EUDAMED last updated this device on May 14, 2026
69415580Medicalk28781KS28781 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Allmed Medical Products Co.,Ltd. Placed on the EU market in Northern Ireland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0501982900561069415580Medicalk28781KS28781(01)05019829005610
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.
V0599CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHERNo certificate specifically references this device's Basic UDI-DI.
Primary placement in XI; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| XIPrimary placement | Still on market |
CN-MF-000007970No 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.