- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 31, 2026
843660129ZPMQ72 references
843660129ZPMQ7Basic 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.
Z12040203Dermal regeneration equipmentZ12062801Muscle reinforcement stimulators for innervated muscles2 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 |
|---|---|---|---|---|---|
| ZIONIC PRO MAX | ZIONIC PRO MAX | M105 | 08436601291356 | 1 | On the market |
| ZIONIC PRO MAX | ZIONIC PRO MAX | M105/1 | 08436601291448 | 1 | On the market |