- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 30, 2026
69370230QYQ-KTB3 references
69370230QYQ-KTBNo 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.
G0308010101Gastrointestinal endoscopy, cold biopsy forceps, single-use3 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 |
|---|---|---|---|---|---|
| VTL/TBC-BFC2-18-120 | — | VTL/TBC-BFC2-18-120 | 06937023078577 | 1 | On the market |
| VTL/BFC2-23-160 | — | VTL/BFC2-23-160 | 06937023078522 | 1 | On the market |
| VTL/BFC2-23-230 | — | VTL/BFC2-23-230 | 06937023078515 | 1 | On the market |