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 4F SL-10cm AST - Rapid Deployment Procedure Basic Kit FDA UDI
Model / Reference: H965460420 FDA UDI
Description: BioFlo Midline with ENDEXO Technology 4F SL-10cm AST - Rapid Deployment Procedure Basic Kit FDA UDI

Identifiers

Catalog Number: 46-042 FDA UDI
Primary DI / UDI-DI: 15051684030007 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: Lumen/Inner Diameter — 0.018 Inch FDA UDI
Outer Diameter — 1.4 Millimeter FDA UDI
Length — 10 Centimeter FDA UDI
Catheter Gauge — 4 French FDA UDI

Category: Peripheral intravenous cannula

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

Similar devices

Also classified as Peripheral intravenous cannula.

McKesson — MCKESSON MEDICAL-SURGICAL INC. · Class II
Supercath 5 — TOGO MEDIKIT CO., LTD. · Class II
Nipro SafeTouch IV Catheter — NIPRO MEDICAL CORPORATION · Class II
BioFlo — NAVILYST MEDICAL, INC. · Class II
Navilyst Medical — NAVILYST MEDICAL, INC.
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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Angiodynamics, Inc.

Sources (1)

FDA UDI 17f12f50-b268-4ee5-a1c5-c75520733ae5 37 fields · synced Jun 8, 2026