- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Jun 8, 2026
B-04772085004148N-ELUTAX “3” is an MDD-legacy medical device registered in EUDAMED. It is classified as Class III. Manufactured by AR Baltic Medical UAB. Placed on the EU market in Lithuania. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
04772085004148B-04772085004148N-ELUTAX “3” 25325(01)04772085004148
European Medical Device Nomenclature — the EU product classification assigned to this device.
C010402020101PTA BALLOON DILATATION CATHETERS4 warnings recorded — scroll inside the panel to see all entries.
CW010CW009CW001CW007No certificate specifically references this device's Basic UDI-DI.
Primary placement in Lithuania; available across 19 countries total.
| Country | On market since | Until |
|---|---|---|
| LithuaniaPrimary placement | Still on market | |
| Austria | Still on market | |
| Bulgaria | Still on market | |
| Cyprus | Still on market | |
| Czechia | Still on market | |
| Germany | Still on market | |
| Estonia | Still on market | |
| EL | Still on market | |
| Spain | Still on market | |
| Croatia | Still on market | |
| Hungary | Still on market | |
| Ireland | Still on market | |
| Iceland | Still on market | |
| Italy | Still on market | |
| Latvia | Still on market | |
| Poland | Still on market | |
| Portugal | Still on market | |
| Slovakia | Still on market | |
| Türkiye | Still on market |
LT-MF-000004402No 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.M.2018.106.9148M.2018.106.9148-1