- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 30, 2026
4031815080904B2 references
4031815080904BNo 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.
M04010101Non-woven adhesive dressings, with absorbent pad2 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 |
|---|---|---|---|---|---|
| RUDADERM®-FINGERKUPPENPFLASTER | RUDADERM®-FINGERKUPPENPFLASTER | 089090 | 04031815080921 | 100 | On the market |
| RUDADERM®-ZEHENPFLASTER | RUDADERM®-ZEHENPFLASTER | 089100 | 04031815081027 | 100 | On the market |