- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 16, 2026
0888937TD015rYF10 references
0888937TD015rYFNo 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 →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.
L059004Uterine manipulators, reusable10 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 |
|---|---|---|---|---|---|
| Advincula Arch® | Advincula Arch® | UMH750 | 00888937015225 | 1 | On the market |
| Koh Cup™ | Koh Cup™ | KCS-30 | 00888937015737 | 1 | On the market |
| Koh Cup™ | Koh Cup™ | KCS-40 | 00888937015751 | 1 | On the market |
| Koh Cup™ | Koh Cup™ | KCS-35 | 00888937015744 | 1 | On the market |
| RUMI® II | RUMI® II | UMH650 | 00888937015232 | 1 | On the market |
| RUMI® II | RUMI® II | UMH650L | 00888937025637 | 1 | On the market |
| Ultem® Koh Cups™ | Ultem® Koh Cups™ | KCP-40-2 | 00888937015720 | 1 | On the market |
| Ultem® Koh Cups™ | Ultem® Koh Cups™ | KCP-35-2 | 00888937015713 | 1 | On the market |
| Ultem® Koh Cups™ | Ultem® Koh Cups™ | KCP-30-2 | 00888937015706 | 1 | On the market |
| KC-SIZER | — | KC-SIZER | 00888937011135 | 1 | On the market |