Deltaven 3810172
Deltaven 3810172 is a Class II device made by Delta Med SpA, listed in FDA GUDID since 19 Jan 2018 (UDI-DI 08032248381018), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number08032248381018 | Date19 Jan 2018 | StatusListed |
Official records
- AccessGUDID record 08032248381018
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Deltaven
- Generic name
- Peripheral vascular catheter
- Model / reference
- 3810172
- Description
- Safety IV Catheter in PUR with closed system, Y final adapter and detachable needless valve
- Primary DI / UDI-DI
- 08032248381018
- FDA product code
- FOZ
- GMDN term
- Peripheral vascular catheter
- Device class
- Class II
- Regulation number
- 880.5200
- GUDID distribution status
- In Commercial Distribution
- Size
- Outer Diameter — 0.74 MillimeterLength — 19 Millimeter
Similar devices
Other devices filed under FDA product code FOZ (Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 Days).
- Medical Components IV Catheter by Medical Components, Inc.
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- Nu-Cath Emergency Kit by Intl. Medical Devices, Ltd.
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- DESERET MULTILUMEN SUBCLAVIAN JUGULAR by Parke-Davis Co.
- Deseret Angio-Guide Large Vein Cath. by Warner-Lambert Co.
- NIPRO SAFELET CATH by Pharma-Plast USA, Inc.
- Cook Five Lumen Central Venous Catheter by Cook, Inc.
- Nexiva Closed IV Catheter System with NearPort IV Access by Becton Dickinson Infusion Therapy Systems Inc.
- Angio-Set Intravenous Cath. Set by Deseret Medical, Inc.