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Argyle

FDA UDI

Class II (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
Argyle FDA UDI
Generic Name
Cardiac ventriculography catheter FDA UDI
Device Name
Agyle Left Ventricular Catheter Ferguson, Radiopaque Line and Eye 18Fr/Ch (6.0 mm) x 20" (51cm) FDA UDI
Model / Reference
8888590018 FDA UDI
Description
Agyle Left Ventricular Catheter Ferguson, Radiopaque Line and Eye 18Fr/Ch (6.0 mm) x 20" (51cm) FDA UDI

Identifiers

Catalog Number
8888590018 FDA UDI
Primary DI / UDI-DI
10192253003734 FDA UDI
FDA Product Code
DWF FDA UDI
GMDN Term
Cardiac ventriculography catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4210 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

No

FDA UDI

Dimensions & Sizes

Size
Length — 20 Inch FDA UDI
Catheter Gauge — 18 French FDA UDI

Category: Cardiac ventriculography catheter

Argyle by Cardinal Health 200, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiac ventriculography catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinal Health 200, LLC

Sources (1)

  • FDA UDI f0683e40-ddb7-4c7e-8450-855deda43ef7 35 fields · synced Jun 8, 2026