- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated May 31, 2026
B-012059LH1 reference
B-012059LHNCT025456081088262021098CE07NCT0471793MA-1700-04NCT02703948NCT06372782Basic 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.
X0303Substances, combinations of substances, or items without an intended medical purpose intended to be used for facial or other dermal or mucous membrane filling by subcutaneous, submucous or intradermal injection or other introduction, by a prefilled means for introduction, excluding those for tattooing – resorbable1 reference
| Product | Trade name | Reference / catalog number | UDI-DI code | Quantity | Status |
|---|---|---|---|---|---|
| Restylane Skinboosters Vital Lidocaine | Restylane Skinboosters Vital Lidocaine | 012059 | D-012059LH | 1 | On the market |