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Fluency® Endovascular Stent Graft

FDA UDI

Class III (US FDA UDI)

by Bard Peripheral Vascular

Identity

Trade Name
Fluency® Endovascular Stent Graft FDA UDI
Generic Name
Central/peripheral venous endovascular stent-graft FDA UDI
Device Name
FLUENCY® PLUS Endovascular Stent Graft 9 mm x 100 mm (117 cm delivery system) FDA UDI
Model / Reference
FEL09100 FDA UDI
Description
FLUENCY® PLUS Endovascular Stent Graft 9 mm x 100 mm (117 cm delivery system) FDA UDI

Identifiers

Catalog Number
FEL09100 FDA UDI
Primary DI / UDI-DI
04049519008219 FDA UDI
FDA Product Code
PFV FDA UDI
GMDN Term
Central/peripheral venous endovascular stent-graft FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Fluency® Endovascular Stent Graft by Bard Peripheral Vascular — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c20a1e19-90ca-4308-8471-3f316dcdb748 37 fields · synced May 30, 2026