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Quikcord

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
QUIKCORD FDA UDI
Generic Name
Polyolefin/fluoropolymer suture, multifilament FDA UDI
Device Name
White/Green Co Braid Size 3.5mm 30" Medshape FDA UDI
Model / Reference
IPN001120 FDA UDI
Description
White/Green Co Braid Size 3.5mm 30" Medshape FDA UDI

Identifiers

Catalog Number
1700-02-000 FDA UDI
Primary DI / UDI-DI
14026704596390 FDA UDI
FDA Product Code
GAT FDA UDI
GMDN Term
Polyolefin/fluoropolymer suture, multifilament FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5000 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Polyolefin/fluoropolymer suture, multifilament

Quikcord by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polyolefin/fluoropolymer suture, multifilament.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI 2389e784-cce6-4940-8a63-8269b838085d 36 fields · synced Jun 8, 2026