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EUDAMED last updated this device on Oct 25, 2024
B-59037695020667EENT14 is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Gofarm Sp. z o.o. Sp. k.. Placed on the EU market in Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
D-59037695020667EB-59037695020667EENT14D-59037695020667E
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.
European Medical Device Nomenclature — the EU product classification assigned to this device.
Q0399ENT DEVICES - OTHER4 warnings recorded — scroll inside the panel to see all entries.
CW010CW032CW007CW999No certificate specifically references this device's Basic UDI-DI.
Primary placement in Poland; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| PolandPrimary placement | Still on market |
PL-MF-000003485Certificate health across this manufacturer's portfolio.
1434-MDR-006/2026Issued1434-MDR-046/2025Issued1434-MDR-045/2025Issued1434-MDR-044/2025Issued1434-MDR-041/2025Amended1434-MDR-042/2025Issued1434-MDD-350/2021