- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Apr 24, 2026
3665023TOF-MUUJ036650230013653665023TOF-MUUJTF2-MU_DR(01)03665023001365
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.
Z1203019001NEUROMUSCULAR RELAXATION MONITORING EQUIPMENT2 warnings recorded — scroll inside the panel to see all entries.
CW011CW014No certificate specifically references this device's Basic UDI-DI.
Primary placement in France; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Still on market |
FR-MF-000002402No 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.