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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, Straight, 4 mm x 40 cm FDA UDI
Model / Reference
40S04 FDA UDI
Description
IMPRA® ePTFE Vascular Graft, Straight, 4 mm x 40 cm FDA UDI

Identifiers

Catalog Number
40S04 FDA UDI
Primary DI / UDI-DI
00801741021817 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
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

Dimensions & Sizes

Size
Length — 40 Centimeter FDA UDI

The IMPRA ePTFE Vascular Graft, a premium solution for cardiovascular procedures, offers a durable and reliable alternative to traditional implants. With its advanced material and manufacturing process, this graft is designed to provide long-lasting performance in a variety of surgical settings.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bard Peripheral Vascular

Sources (1)

  • FDA UDI 1d617760-9e29-4cc1-9766-bfcc18c6a5d6 37 fields · synced Jul 29, 2026