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EUDAMED last updated this device on May 29, 2026
6947462411111230LPCentrifuge tube is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Zhejiang Gongdong Medical Technology Co., Ltd.,. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
069474624390516947462411111230LPD1001G(01)06947462439051
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.
W05019099SAMPLES COLLECTION DEVICES - OTHERNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Germany; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Still on market |
CN-MF-000005694Certificate health across this manufacturer's portfolio.
G10 042464 0037Issued