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EUDAMED last updated this device on May 3, 2022
B-ITMF000013510H160018EH16001 is an MDD-legacy medical device registered in EUDAMED. It is classified as Class III. Manufactured by NYUMA PHARMA S.R.L.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
D-ITMF000013510H160018EB-ITMF000013510H160018EH16001D-ITMF000013510H160018E
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.
European Medical Device Nomenclature — the EU product classification assigned to this device.
P900402RESORBABLE FILLING AND RECONSTRUCTION DEVICES5 warnings recorded — scroll inside the panel to see all entries.
CW010CW001CW007CW011CW135No certificate specifically references this device's Basic UDI-DI.
Primary placement in Italy; available across 11 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Still on market | |
| Austria | Still on market | |
| Belgium | Still on market | |
| Czechia | Still on market | |
| EL | Still on market | |
| Spain | Still on market | |
| France | Still on market | |
| Poland | Still on market | |
| Portugal | Still on market | |
| Romania | Still on market | |
| Türkiye | Still on market |
IT-MF-000013510No 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.EPG-0308-20QCT-0161-20