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Gelweave™

FDA UDI

Class II (US FDA UDI)

by Vascutek Ltd

Identity

Trade Name
Gelweave™ FDA UDI
Generic Name
Synthetic vascular graft FDA UDI
Device Name
Gelweave Gelatin Impregnated Woven Vascular Prosthesis STRAIGHT FDA UDI
Model / Reference
731510 FDA UDI
Description
Gelweave Gelatin Impregnated Woven Vascular Prosthesis STRAIGHT FDA UDI

Identifiers

Catalog Number
731510 FDA UDI
Primary DI / UDI-DI
05037881105086 FDA UDI
FDA Product Code
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

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 15 Centimeter FDA UDI
Lumen/Inner Diameter — 10 Millimeter FDA UDI

Category: Synthetic vascular graft

Gelweave™ by Vascutek Ltd — 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

Manufacturer
Vascutek Ltd

Sources (1)

  • FDA UDI 401fe9ea-4cbd-458b-b79a-57ebe61d95b0 37 fields · synced May 30, 2026