- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jun 21, 2026
B-USMF000054278BMCXJ020HP1 reference
B-USMF000054278BMCXJ020HPBM-PRD-PRO-CSP-77VALREP19-009REP19-010REP19-012Basic 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.
W0106010109Sickle cell anemia1 reference
| Product | Trade name | Reference / catalog number | UDI-DI code | Quantity | Status |
|---|---|---|---|---|---|
| Sickle SCAN Test | Sickle SCAN Test | CXJ020 | D-USMF000054278BMCXJ020HP | 1 | On the market |