LuxInject syringe
by Margomed Spółka Akcyjna 5 variants
Ref 010 100, 010 050, 010 020, 010 201, 010 102, 010 022, 010 052, 010 051Model LuxInject syringe, ProInject syringe
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number59045539930101WA | Date10 Sep 2025 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Syringe
- Model / Reference
- LuxInject syringe, ProInject syringe, 010 100, 010 050, 010 020, 010 201, 010 102, 010 022, 010 052, 010 051
- Primary DI / UDI-DI
- 05904553993060, 05904553993053, 05904553993046, 05905386929615, 05907269030012, 05905386929998, 05907269030005, 05905386929592
- Basic UDI-DI
- 59045539930101WA
- EMDN Code
- A020199 Syringes, single-use - other
- Device Class
- Class IIa
- EU market of registration
- Poland
Manufacturer details
- EUDAMED SRN
- PL-MF-000009261
Other devices from Margomed Spółka Akcyjna
Properties
Other properties (11)
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Incorporates Medicinal Product: No