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EUDAMED last updated this device on May 14, 2026
8005830GNPFYYESNC/XL is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by ICOGUANTI S.p.A.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
080058300027908005830GNPFYYESNC/XL(01)08005830002790
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.
T01020204NITRILE EXAMINATION / TREATMENT GLOVES1 warning recorded — scroll inside the panel to see all entries.
CW129No certificate specifically references this device's Basic UDI-DI.
Primary placement in Italy; available across 5 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Oct 24, 2022 | Still on market |
| Germany | Oct 24, 2022 | Still on market |
| Spain | Oct 24, 2022 | Still on market |
| France | Oct 24, 2022 | Still on market |
| Poland | Oct 24, 2022 | Still on market |
IT-MF-000053804No 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.