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- Date of registration
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EUDAMED last updated this device on May 25, 2026
B-06931132222210Sequasorb Ag+ is an MDD-legacy medical device registered in EUDAMED. It is classified as Class III. Manufactured by Foshan United Medical Technologies Ltd.. Placed on the EU market in Greece. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06931132222210B-06931132222210AG1419(01)06931132222210
European Medical Device Nomenclature — the EU product classification assigned to this device.
M04040801SILVER DRESSINGS, NON-COMBINED2 warnings recorded — scroll inside the panel to see all entries.
CW010CW027No certificate specifically references this device's Basic UDI-DI.
Primary placement in EL; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| ELPrimary placement | Aug 10, 2025 | Still on market |
CN-MF-000017922No 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.596672