- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Apr 2, 2026
805551056cont_precarAT1589 is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Kaltek S.r.l.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
08055510563080805551056cont_precarAT1589(01)08055510563080
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.
W050301029099SAMPLES ANALYSES, PLASTIC CONTAINERS - OTHERNo 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 | Still on market | |
| Estonia | Still on market | |
| Spain | Still on market | |
| Netherlands | Still on market | |
| Poland | Still on market |
IT-MF-000019573Certificate health across this manufacturer's portfolio.
IT348898Issued0425-MDR-030116-00Issued