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- Date of registration
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EUDAMED last updated this device on Feb 11, 2026
5900516AAKXXXXUDPL-MF-000002200Certificate health across this manufacturer's portfolio.
TNP/MDR/0035/4722/2025AmendedTNP/MDR/0036/4722/2025Issued4 warnings recorded — scroll inside the panel to see all entries.
CW007CW009CW011CW032Primary placement in Poland; available across 20 countries total.
| Country | On market since | Until |
|---|---|---|
| PolandPrimary placement | Still on market | |
| Austria | Still on market | |
| Belgium | Still on market | |
| Czechia | Still on market | |
| Germany | Still on market | |
| Estonia | Still on market | |
| Spain | Still on market | |
| France | Still on market | |
| Hungary | Still on market | |
| Ireland | Still on market | |
| Italy | Still on market | |
| Liechtenstein | Still on market | |
| Lithuania | Still on market | |
| Luxembourg | Still on market | |
| Latvia | Still on market | |
| Malta | Still on market | |
| Netherlands | Still on market | |
| Portugal | Still on market | |
| Romania | Still on market | |
| Slovakia | Still on market |
(01)05900516738273
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