Identity
- Trade Name
- NEOFLON EUDAMED
- Device Name
- BD Neoflon™ Pro IV Cannula EUDAMED
- Model / Reference
- 391389 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 30382903913894 EUDAMED
- Basic UDI-DI
- 038290ZCNOSRXLMV EUDAMED
- Unit of Use DI
- 00382903913893 EUDAMED
- EMDN Code
- C0101010101 PERIPHERAL I.V. CATHETERS, W/O SAFETY SYSTEMS, WITH INJECTION VALVES EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Lithuania EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
Yes
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
Yes
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
Yes
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Neoflon by Becton Dickinson Infusion Therapy Systems Inc. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 038290ZCNOSRXLMV | Class IIa | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Becton Dickinson Infusion Therapy Systems Inc.
- EUDAMED SRN
- US-MF-000017719
- Authorised Representative
- Becton Dickinson Ireland Limited IE-AR-000007610
Sources (1)
- EUDAMED 970cfab4-65fe-4ddd-8add-01271a426080 61 fields · synced Jun 17, 2026