Vacusera
by Di̇sera Tibbi̇ Malzeme Loji̇sti̇k San. Ve Ti̇c. A.Ş. 83 variants
Ref 2392118N
Active
CE MDR CE MDD
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 | NumberB-M7122392118N1 | Date8 Nov 2023 | StatusActive |
| European Union | CE/MDD | NumberB-M7122392118N1 | Date8 Nov 2023 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR, CE/MDD Active
Specification
- Device Name
- VACUSERA® Pressure Activated Safety Blood Lancet 21G 1,8 mmVACUSERA® Pressure Activated Safety Blood Lancet
- Model / Reference
- 2392118N
- Primary DI / UDI-DI
- M7122392118N1, +M7122392118N1.
- Basic UDI-DI
- B-M7122392118N1, ++M712239LANCETE8
- Direct Marketing DI
- +M7122392118N1.
- EMDN Code
- V010401 Lancets with safety systems, single-use
- Device Class
- Class IIa
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- TR-MF-000025066
Other devices from Di̇sera Tibbi̇ Malzeme Loji̇sti̇k San. Ve Ti̇c. A.Ş.
See all devices from Di̇sera Tibbi̇ Malzeme Loji̇sti̇k San. Ve Ti̇c. A.Ş. →
Properties
Other properties (12)
- 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
- Measuring Function: No
- Incorporates Medicinal Product: No