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GORE PROPATEN Vascular Graft

FDA UDI

Class II (US FDA UDI)

by W. L. Gore & Associates, Inc

Identity

Trade Name
GORE PROPATEN Vascular Graft FDA UDI
Generic Name
Synthetic vascular graft FDA UDI
Device Name
PROPATEN VASCULAR GRAFT TW IR 7mmX60cm 60cm Rings Heparin FDA UDI
Model / Reference
IRTH076060A FDA UDI
Description
PROPATEN VASCULAR GRAFT TW IR 7mmX60cm 60cm Rings Heparin FDA UDI

Identifiers

Catalog Number
IRTH076060A FDA UDI
Primary DI / UDI-DI
00733132607402 FDA UDI
FDA Product Code
DSY FDA UDI
DYF 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

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Lumen/Inner Diameter — 7 Millimeter FDA UDI
Length — 60 Centimeter FDA UDI

Category: Synthetic vascular graft

GORE PROPATEN Vascular Graft by W. L. Gore & Associates, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Synthetic vascular graft.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5518e228-c972-4cf8-8553-118fee79d2c2 36 fields · synced Jun 1, 2026