IMPRA® ePTFE Vascular Grafts

FDA UDI

Class II (US FDA UDI)

by Bard Peripheral Vascular

Identity

Trade Name: IMPRA® ePTFE Vascular Grafts FDA UDI
Generic Name: Synthetic vascular graft FDA UDI
Device Name: IMPRA® ePTFE Vascular Graft, Carboflo® Short Tapered Carbon-Lined, 7-4 mm x 40 cm FDA UDI
Model / Reference: 40A74C FDA UDI
Description: IMPRA® ePTFE Vascular Graft, Carboflo® Short Tapered Carbon-Lined, 7-4 mm x 40 cm FDA UDI

Identifiers

Catalog Number: 40A74C FDA UDI
Primary DI / UDI-DI: 00801741021008 FDA UDI
FDA Product Code: DYF FDA UDI
DSY FDA UDI
GMDN Term: Synthetic vascular graft FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.3450 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

Dimensions & Sizes

Size: Length — 40 Centimeter FDA UDI

Category: Synthetic vascular graft

IMPRA® ePTFE Vascular Grafts by Bard Peripheral Vascular — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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COOK — William Cook Europe ApS · Class III
Gelweave™ — VASCUTEK LTD · Class II
Zenith — WILLIAM A. COOK AUSTRALIA PTY. LTD. · Class III
ADVANTA SLIDER GDS — Atrium Medical Corp. · Class II
Gelweave Vascular Prostheses — VASCUTEK LTD · 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 868982c6-b31a-4fc7-bd45-71925ea81a5f 36 fields · synced May 30, 2026