BD Intraosseous Vascular Access System

FDA UDI

Class II (US FDA UDI)

by Bard Access Systems, Inc.

Identity

Trade Name: BD Intraosseous Vascular Access System FDA UDI
Generic Name: Intraosseous infusion kit FDA UDI
Device Name: BD Intraosseous Manual Driver FDA UDI
Model / Reference: D015151MK FDA UDI
Description: BD Intraosseous Manual Driver FDA UDI

Identifiers

Catalog Number: D015151MK FDA UDI
Primary DI / UDI-DI: 00801741163623 FDA UDI
FDA Product Code: FMI FDA UDI
GMDN Term: Intraosseous infusion kit FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5570 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

Yes

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

MRI Safety

MR Unsafe FDA UDI

Dimensions & Sizes

Size: Needle Gauge — 15 Gauge FDA UDI
Length — 15 Millimeter FDA UDI

Category: Intraosseous infusion kit

BD Intraosseous Vascular Access System by Bard Access Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Bard Access Systems, Inc.

Sources (1)

FDA UDI ecdaa562-2a10-4f39-8693-573aaef6d9dc 36 fields · synced Jun 9, 2026