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EUDAMED last updated this device on Apr 22, 2026
69367337LP0024MLAngiopower™ is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Lepu Medical Technology (Beijing) Co., Ltd.. Placed on the EU market in Lithuania. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0693673379411169367337LP0024MLLP-P-30S(01)06936733794111
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.
C0104010280INTERVENTIONAL CORONARY ANGIOGRAPHY DEVICES - ACCESSORIES1 warning recorded — scroll inside the panel to see all entries.
CW010No certificate specifically references this device's Basic UDI-DI.
Primary placement in Lithuania; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| LithuaniaPrimary placement | Mar 7, 2019 | Still on market |
CN-MF-000001408Certificate health across this manufacturer's portfolio.
HZ 2111879-1IssuedDZ 2111879-1Cancelled