- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 29, 2026
695238330003GF06952383306443695238330003GF1000ml(01)06952383306443
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.
W0103010301HISTO / CYTO STAINSNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Germany; available across 1 country total.
Placed on the market in Germany; per-country availability dates not published.
CN-MF-000050424No 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.