Venflon
by Becton Dickinson Infusion Therapy Systems Inc. 72 variants
Ref 393243
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 | Number038290CRHGWSVQC6 30382903932437 | Date6 Jun 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- Withdrawn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
- BD Venflon™ Pro IV Cannula with BD Instaflash™ Needle Technology
- Model / Reference
- 393243
- Primary DI / UDI-DI
- 30382903932437
- Basic UDI-DI
- 038290CRHGWSVQC6
- Unit of Use DI
- 00382903932436
- EMDN Code
- C0101010101 Peripheral i.v. catheters, w/o safety systems, with injection valves
- Device Class
- Class IIa
- EU market of registration
- France
Manufacturer details
- EUDAMED SRN
- US-MF-000017719
- Authorised representative
- Becton Dickinson Ireland Limited IE-AR-000007610
Other devices from Becton Dickinson Infusion Therapy Systems Inc.
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Properties
Other properties (10)
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Measuring Function: No
- Incorporates Medicinal Product: No