- Role
- Country
- Date of registration
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EUDAMED last updated this device on Jun 8, 2026
697049309W01030000009A806970493096702697049309W01030000009A812.01.1419A(01)06970493096702
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.
W0103010105CBC-REAGENTS (CLEANING-/DILUTING-/LYSING-/SHEAT-FLUIDS)1 warning recorded — scroll inside the panel to see all entries.
CW011No 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 | Jun 28, 2024 | Dec 31, 2099 |
CN-MF-000024842No 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-06941377306453On the marketActivated Partial Thromboplastin Time Assay Kit(Ellagic Acid)(Coagulation Method)B-06941377306521On the marketActivated Partial Thromboplastin Time Assay Kit(Ellagic Acid)(Coagulation Method)B-06941377306507On the marketActivated Partial Thromboplastin Time Assay Kit(Ellagic Acid)(Coagulation Method)B-06941377306514On the marketActivated Partial Thromboplastin Time Assay Kit(Ellagic Acid)(Coagulation Method)B-06941377306491On the market