LifeStent® Vascular & Biliary Stent

FDA UDI

Class II (US FDA UDI)

by Bard Peripheral Vascular

Identity

Trade Name: LifeStent® Vascular & Biliary Stent FDA UDI
Generic Name: Peripheral artery stent, bare-metal FDA UDI
Device Name: BARD® LIFESTENT® Vascular and Biliary Stent System 7 mm x 40 mm (80 cm delivery catheter) FDA UDI
Model / Reference: EX070401CS FDA UDI
Description: BARD® LIFESTENT® Vascular and Biliary Stent System 7 mm x 40 mm (80 cm delivery catheter) FDA UDI

Identifiers

Catalog Number: EX070401CS FDA UDI
Primary DI / UDI-DI: 04049519001081 FDA UDI
FDA Product Code: FGE FDA UDI
NIP FDA UDI
GMDN Term: Peripheral artery stent, bare-metal FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 876.5010 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

MRI Safety

MR Conditional FDA UDI

Category: Peripheral artery stent, bare-metal Bare-metal biliary stent

LifeStent® Vascular & Biliary Stent by Bard Peripheral Vascular — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bare-metal biliary stent.

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SMART FLEX — Cordis US Corp. · Class II
BONASTENT® Biliary — Sewoon Medical Co., Ltd. · Class II
Palmaz BLUE Transhepatic Biliary Stent on SLALOM .018 System — Cordis US Corp. · Class II
Protégé™ GPS™ — EV3, INC · Class II
PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035" Delivery System — Cordis US Corp. · Class II
Protege GPS — Covidien LP · 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: Bard Peripheral Vascular

Sources (1)

FDA UDI 99be6731-190c-4002-8800-70770b51e2ee 37 fields · synced Jun 1, 2026