- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 31, 2026
5690967BU00031N49 references
5690967BU00031N4No 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.
Y06120601Passive ankle-foot orthoses9 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 |
|---|---|---|---|---|---|
| AirForm® Night Splint | AirForm® Night Splint | 50045I | 05690977704688 | 1 | On the market |
| AirForm® Night Splint | AirForm® Night Splint | 50047 | 05690977163614 | 1 | On the market |
| AirForm® Night Splint | AirForm® Night Splint | 50045 | 05690977163553 | 1 | On the market |
| AirForm® Night Splint | AirForm® Night Splint | 50047I | 05690977704695 | 1 | On the market |
| Exoform® Dorsal Night Splint | Exoform® Dorsal Night Splint | W-50087 | 05690977195288 | 1 | On the market |
| Exoform® Dorsal Night Splint | Exoform® Dorsal Night Splint | W-50085 | 05690977195271 | 1 | On the market |
| Formfit® Night Splint | Formfit® Night Splint | 50023 | 05690967106676 | 1 | On the market |
| Formfit® Night Splint | Formfit® Night Splint | 50025 | 05690977163492 | 1 | On the market |
| Formfit® Night Splint | Formfit® Night Splint | 50027 | 05690977163522 | 1 | On the market |