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Argyle

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Argyle FDA UDI
Generic Name
Cardiac ventriculography catheter FDA UDI
Device Name
Left Ventricular Sump Vent Catheter FDA UDI
Model / Reference
8888590224 FDA UDI
Description
Left Ventricular Sump Vent Catheter FDA UDI

Identifiers

Primary DI / UDI-DI
10884521124585 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
Catheter Gauge — 20 French FDA UDI

Category: Cardiac ventriculography catheter

Argyle by Cardinalhealth — 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
Cardinalhealth

Sources (1)

  • FDA UDI e43a09e2-dfdb-4479-8125-2d7dd6c8e9e4 35 fields · synced May 30, 2026