MEDRAD® Avanta Multi-Patient Disposable Syringe
Ref AVA 500 SYR (Part 1 of 2)
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 | Number0616258TFCN-0101IIaWF 00616258024370 | Date5 Feb 2026 | 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- Withdrawn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
- MEDRAD® Avanta Fluid Management System Disposables
- Model / Reference
- AVA 500 SYR (Part 1 of 2)
- Primary DI / UDI-DI
- 00616258024370
- Basic UDI-DI
- 0616258TFCN-0101IIaWF
- EMDN Code
- A02010401 Syringes for contrast media injector, single-use
- Device Class
- Class IIa
- EU market of registration
- Netherlands
Manufacturer details
- EUDAMED SRN
- US-MF-000007050
- Authorised representative
- Bayer Medical Care B.V. NL-AR-000000240
Other devices from Bayer Medical Care Inc.
Properties
Other properties (11)
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No