Vacusera
by Di̇sera Tibbi̇ Malzeme Loji̇sti̇k San. Ve Ti̇c. A.Ş. 217 variants
Ref 234102
Active
CE IVDR CE IVDD
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/IVDR | NumberB-M7122341021 | Date21 Nov 2023 | StatusActive |
| European Union | CE/IVDD | NumberB-M7122341021 | Date21 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- Withdrawn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/IVDR, CE/IVDD Active
Specification
- Device Name
- VACUSERA® 2 ml Z No Additive Blood Collection TubeVACUSERA® Blood Collection Tube
- Model / Reference
- 234102
- Primary DI / UDI-DI
- M7122341021, +M71223410210
- Basic UDI-DI
- B-M7122341021, ++M712234BLOODTUBEG7
- Direct Marketing DI
- +M71223410210
- EMDN Code
- W050101010201, W050101010202
- Device Class
- Class IVD GeneralClass A
- 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 (10)
- Human Tissues: No
- Animal Tissues: No
- Microbial Substances: No
- Reagent: No
- Self Testing: No
- Near-Patient Testing: No
- Professional Testing: No
- Companion Diagnostics: No
- Surgical Instrument: No
- New Device: No