Deltaven Fast Flash

FDA UDI

Class II (US FDA UDI)

by Delta Med Spa

Identity

Trade Name: Deltaven Fast Flash FDA UDI
Generic Name: Peripheral intravenous cannula FDA UDI
Device Name: Safety IV catheter in PUR with closed system, single entry with needleless valve FDA UDI
Model / Reference: 3835373 FDA UDI
Description: Safety IV catheter in PUR with closed system, single entry with needleless valve FDA UDI

Identifiers

Primary DI / UDI-DI: 08032248005495 FDA UDI
FDA Product Code: FOZ FDA UDI
GMDN Term: Peripheral intravenous cannula 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 1.00 Millimeter FDA UDI
Length — 25 Millimeter FDA UDI

Category: Peripheral intravenous cannula

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

Similar devices

Also classified as Peripheral intravenous cannula.

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McKesson — MCKESSON MEDICAL-SURGICAL INC. · Class II
Navilyst Medical — NAVILYST MEDICAL, INC.
McKesson — MCKESSON MEDICAL-SURGICAL INC. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Delta Med Spa

Sources (1)

FDA UDI 2d6884e3-23bf-4943-a9e3-22731e2f229c 34 fields · synced Jun 1, 2026