- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 28, 2026
6954152720231AsJCXGQL169541527601256954152720231AsJCXGQL6012(01)16954152760125
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.
W050101010201BLOOD COLLECTION, TUBES WITH ADDITIVES OR SERUM SEPARATOR4 warnings recorded — scroll inside the panel to see all entries.
CW010CW030CW007CW009No 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-000006505No 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.