- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated May 31, 2026
803304054EFGELECGBP3 references
803304054EFGELECGBPNo 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.
V9099Various devices not included in other classes - other3 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 |
|---|---|---|---|---|---|
| ECG & EEG gel "Transound®" | ECG & EEG gel "Transound®" | 61.005.08 | 08033040545400 | 1 | On the market |
| ECG & EEG gel "Transound®" | ECG & EEG gel "Transound®" | 61.250.02 | 08033040545509 | 1 | On the market |
| ECG & EEG spray "Transound®" | ECG & EEG spray "Transound®" | 61.250.19 | 08033040545479 | 1 | On the market |