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Argyle

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Argyle FDA UDI
Generic Name
Carotid artery shunt FDA UDI
Device Name
Carotid Artery Shunt Kit;Radiopaque Line, Straight FDA UDI
Model / Reference
8888577775 FDA UDI
Description
Carotid Artery Shunt Kit;Radiopaque Line, Straight FDA UDI

Identifiers

Catalog Number
8888577775 FDA UDI
Primary DI / UDI-DI
10884521124547 FDA UDI
FDA Product Code
DWF FDA UDI
GMDN Term
Carotid artery shunt 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

Category: Carotid artery shunt

Argyle by Cardinalhealth — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Carotid artery shunt.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI ac3bd5d2-c9b9-43d5-9868-0106b9865bb0 36 fields · synced May 31, 2026