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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-access handpiece, infusion, electric FDA UDI
Device Name
BD Intraosseous Powered Driver (Refurb) FDA UDI
Model / Reference
D001001R FDA UDI
Description
BD Intraosseous Powered Driver (Refurb) FDA UDI

Identifiers

Catalog Number
D001001R FDA UDI
Primary DI / UDI-DI
00801741201073 FDA UDI
FDA Product Code
FMI FDA UDI
GMDN Term
Intraosseous-access handpiece, infusion, electric 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Intraosseous-access handpiece, infusion, electric

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

Similar devices

Also classified as Intraosseous-access handpiece, infusion, electric.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bard Access Systems, Inc.

Sources (1)

  • FDA UDI 27069086-f646-475e-8f6a-a02095c67025 36 fields · synced Jun 9, 2026