- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 8, 2026
570748030100804308Z6 references
570748030100804308ZNo device characteristics flagged
Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →SRN
An SRN is the unique EUDAMED identifier assigned to a manufacturer, authorised representative or importer when it registers as an actor.
View in glossary →European Medical Device Nomenclature — the EU product classifications carried across this device family's references.
N010101Electromyographic electrodes6 references
| Product | Trade name | Reference / catalog number | Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary → | Quantity | Status |
|---|---|---|---|---|---|
| Ambu® Neuroline Inoject | Ambu® Neuroline Inoject | 74430-36/10 | 05707480023820 | 1 | On the market |
| Ambu® Neuroline Inoject | Ambu® Neuroline Inoject | 74438-45/10 | 05707480023837 | 1 | On the market |
| Ambu® Neuroline Inoject | Ambu® Neuroline Inoject | 74435-40/10 | 05707480024155 | 1 | On the market |
| Ambu® Neuroline Inoject | Ambu® Neuroline Inoject | 74450-50/10 | 05707480023844 | 1 | On the market |
| Ambu® Neuroline Inoject | Ambu® Neuroline Inoject | 74475-55/10 | 05707480023851 | 1 | On the market |
| Ambu® Neuroline Inoject | Ambu® Neuroline Inoject | 74425-30/10 | 05707480023813 | 1 | On the market |