- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 15, 2026
0845357001236WP4 references
0845357001236WPBasic 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.
W01040601Qc strains bacteriology4 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 |
|---|---|---|---|---|---|
| [01236L] LYFO DISK™ V. parahaemolyticus (o2:k3) NCTC 10885 | — | [01236L] LYFO DISK™ V. parahaemolyticus (o2:k3) NCTC 10885 | 10845357040104 | 1 | On the market |
| [01236K] KWIK-STIK™ V. parahaemolyticus (o2:k3) NCTC 10885 | — | [01236K] KWIK-STIK™ V. parahaemolyticus (o2:k3) NCTC 10885 | 30845357040092 | 1 | On the market |
| [01236U] KWIK-STIK™ V. parahaemolyticus (o2:k3) NCTC 10885 | — | [01236U] KWIK-STIK™ V. parahaemolyticus (o2:k3) NCTC 10885 | 10845357040081 | 1 | On the market |
| [01236P] KWIK-STIK™ V. parahaemolyticus (o2:k3) NCTC 10885 | — | [01236P] KWIK-STIK™ V. parahaemolyticus (o2:k3) NCTC 10885 | 20845357040088 | 1 | On the market |