- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 18, 2026
8005830GLPFYNIT-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.1 warning recorded — scroll inside the panel to see all entries.
CW129Primary placement in Italy; available across 5 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Sep 12, 2022 | Still on market |
| Germany | Sep 12, 2022 | Still on market |
| Spain | Sep 12, 2022 | Still on market |
| France | Sep 12, 2022 | Still on market |
| Poland | Sep 12, 2022 | Still on market |
(01)08005830010597
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.
T010201LATEX EXAMINATION / TREATMENT GLOVES