- Role
- Country
- Date of registration
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EUDAMED last updated this device on Jul 21, 2025
59026439BRTDOA1105012SFPL-MF-000039473No 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.Primary placement in Poland; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| PolandPrimary placement | Still on market |
(01)05902643959187
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.
W0102160511MULTIPLE DRUGS OF ABUSE/TOXICOLOGY RT & POC