- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 30, 2026
69503348PAA005FF0695033481948669503348PAA005FFPA480(01)06950334819486
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.
W0201020102AUTOMATED IMMUNOCHEMISTRY ANALYSERS - MODERATE ROUTINE (Throughput > 100 and <= 250 test/h)No certificate specifically references this device's Basic UDI-DI.
Primary placement in Türkiye; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| TürkiyePrimary placement | Still on market |
CN-MF-000017351No 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.B-06950334802334On the market25-OH Vitamin D (25-OH Vit-D) Quality ControlB-06950334815044On the market25-OH Vitamin D (25-OH Vit-D) Test Kit (Immunofluorescence)B-06950334821991On the marketAlpha Fetoprotein (AFP) Test Kit (Immunofluorescence)B-06950334813798On the marketAnti-streptolysin O (ASO) Detection Kit (Nephelometry)B-06950334819646On the market