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EUDAMED last updated this device on Jun 9, 2026
69449040AB74000715TAngiotensin Ⅱ(CLIA) is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class B. Manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0690305309378169449040AB74000715T105-049532-00(01)06903053093781
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.
W0102060202ANGIOTENSIN I / IINo certificate specifically references this device's Basic UDI-DI.
Primary placement in Germany; available across 2 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Jan 28, 2026 | Still on market |
| Netherlands | Jan 28, 2026 | Still on market |
CN-MF-000014156Certificate health across this manufacturer's portfolio.
CN26/00002236IssuedCN24/00005514IssuedCN24/00005514IssuedCN23/00003444Supplemented