- Role
- Country
- Date of registration
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EUDAMED last updated this device on Jun 5, 2026
8431673TLTF402R084316731710188431673TLTF402R1107101(01)08431673171018
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.
W01021109C-REACTIVE PROTEIN1 warning recorded — scroll inside the panel to see all entries.
CW010No certificate specifically references this device's Basic UDI-DI.
Primary placement in Spain; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| SpainPrimary placement | Still on market |
ES-MF-000011023Certificate health across this manufacturer's portfolio.
HX 1552211-1Issued