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GORE-TEX Suture

FDA UDI

Class II (US FDA UDI)

by W. L. Gore & Associates, Inc

Identity

Trade Name
GORE-TEX Suture FDA UDI
Generic Name
Polyolefin/fluoropolymer suture, monofilament FDA UDI
Device Name
GORE-TEX SUTURE CV-3 91cm DoubleArm TT-17-1dz FDA UDI
Model / Reference
3N02 FDA UDI
Description
GORE-TEX SUTURE CV-3 91cm DoubleArm TT-17-1dz FDA UDI

Identifiers

Catalog Number
3N02 FDA UDI
Primary DI / UDI-DI
00733132628681 FDA UDI
PMA Number
P820083 FDA UDI
FDA Product Code
GAW FDA UDI
GMDN Term
Polyolefin/fluoropolymer suture, monofilament FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5010 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 91 Centimeter FDA UDI

Category: Polyolefin/fluoropolymer suture, monofilament

GORE-TEX Suture by W. L. Gore & Associates, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polyolefin/fluoropolymer suture, monofilament.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 765baf6f-8cee-43ac-9753-c8144093cb02 37 fields · synced Jun 8, 2026