- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated May 30, 2026
B-4010PAEDGJ1 reference
B-4010PAEDGJBasic 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.
W0102080201CarbamazepineW0102080202EthosuximideW0102080207PhenobarbitalW0102080208PhenytoinW0102080210Valproic acidW0102080212LamotrigineW0102080215LevetiracetamW0102080299Central nervous system tdm - other1 reference
| 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 |
|---|---|---|---|---|---|
| Anti-Epileptic Drugs Basic Panel Reagent Set | Anti-Epileptic Drugs Basic Panel Reagent Set | 4010 P AED | D-4010PAEDGJ | 1 | On the market |