- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 31, 2026
571488270075FV6 references
571488270075FVNo 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.
Y99Devices for persons with disabilities not included in other categories - other6 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 |
|---|---|---|---|---|---|
| Protac KneedMe | Protac KneedMe | 700-751-3820-30 | 05714882012956 | 1 | On the market |
| Protac KneedMe | Protac KneedMe | 700-751-3820-40 | 05714882012970 | 1 | On the market |
| Protac KneedMe | Protac KneedMe | 700-751-3820-41 | 05714882012994 | 1 | On the market |
| Protac KneedMe To Go | Protac KneedMe To Go | 700-755-U-3820-80 | 05714882013076 | 1 | On the market |
| Protac KneedMe To Go | Protac KneedMe To Go | 700-755-U-3820-30 | 05714882013038 | 1 | On the market |
| Protac KneedMe To Go | Protac KneedMe To Go | 700-755-U-3820-40 | 05714882013052 | 1 | On the market |