Langston

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name: LANGSTON FDA UDI
Generic Name: Angiographic catheter, single-use FDA UDI
Device Name: Langston V2, 6F Pigtail FDA UDI
Model / Reference: IPN923473 FDA UDI
Description: Langston V2, 6F Pigtail FDA UDI

Identifiers

Catalog Number: 5540 FDA UDI
Primary DI / UDI-DI: 10841156109158 FDA UDI
FDA Product Code: DQO FDA UDI
GMDN Term: Angiographic catheter, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.1200 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Catheter Gauge — 6 French FDA UDI
Length — 110 Centimeter FDA UDI

Category: Angiographic catheter, single-use

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

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Also classified as Angiographic catheter, single-use.

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ConcierGE Guiding Excellence™ — Merit Medical Systems, Inc. · Class II
INFINITI — Cordis US Corp. · Class II
CXI — COOK INCORPORATED · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Teleflex Incorporated

Sources (1)

FDA UDI b6fd2dee-bcf0-4e99-a1b5-65a7aa9f2410 36 fields · synced May 30, 2026