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Deltaven

FDA UDI

Class II (US FDA UDI)

by Delta Med Spa

Identity

Trade Name
DELTAVEN FDA UDI
Generic Name
Peripheral vascular catheter FDA UDI
Device Name
Safety I.V Catheter in PUR with closed system and detachable stopcock with needless valve FDA UDI
Model / Reference
3845472 FDA UDI
Description
Safety I.V Catheter in PUR with closed system and detachable stopcock with needless valve FDA UDI

Identifiers

Primary DI / UDI-DI
08032248384545 FDA UDI
FDA Product Code
FOZ FDA UDI
GMDN Term
Peripheral vascular catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 25 Millimeter FDA UDI
Outer Diameter — 1.30 Millimeter FDA UDI

Category: Peripheral vascular catheter

Deltaven by Delta Med Spa — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral vascular catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Delta Med Spa

Sources (1)

  • FDA UDI a46e71ec-8dd9-4125-b90d-d9e4d19a4344 34 fields · synced Jun 1, 2026