BioFlo

FDA UDI

Class II (US FDA UDI)

by Angiodynamics, Inc

Identity

Trade Name: BioFlo FDA UDI
Generic Name: Peripheral intravenous cannula FDA UDI
Device Name: BioFlo Midline with ENDEXO Technology 3F SL-10cm AST - Rapid Deployment Procedure Full Kit FDA UDI
Model / Reference: H965460330 FDA UDI
Description: BioFlo Midline with ENDEXO Technology 3F SL-10cm AST - Rapid Deployment Procedure Full Kit FDA UDI

Identifiers

Catalog Number: 46-033 FDA UDI
Primary DI / UDI-DI: 15051684029995 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

FDA UDI

Dimensions & Sizes

Size: Catheter Gauge — 3 French FDA UDI
Length — 10 Centimeter FDA UDI
Outer Diameter — 1.02 Millimeter FDA UDI
Lumen/Inner Diameter — 0.018 Inch FDA UDI

Category: Peripheral intravenous cannula

BioFlo by Angiodynamics, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Angiodynamics, Inc

Sources (1)

FDA UDI 6ed13ee4-af6a-4969-b7e1-71d69a0ac5ae 37 fields · synced Jun 20, 2026