Argyle

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name: Argyle FDA UDI
Generic Name: Closed-wound drain, non-bioabsorbable FDA UDI
Device Name: Thoracic PVC Catheter FDA UDI
Model / Reference: 8888570358 FDA UDI
Description: Thoracic PVC Catheter FDA UDI

Identifiers

Catalog Number: 8888570358 FDA UDI
Primary DI / UDI-DI: 10884521156531 FDA UDI
FDA Product Code: JOL FDA UDI
GMDN Term: Closed-wound drain, non-bioabsorbable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.6740 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

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Length — 20 Inch FDA UDI
Catheter Gauge — 32 French FDA UDI

Category: Closed-wound drain, non-bioabsorbable

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

Similar devices

Also classified as Closed-wound drain, non-bioabsorbable.

Argyle — Cardinal Health 200, LLC · Class II
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One-Step™ — Merit Medical Systems, Inc. · Class I
Argyle — Cardinal Health 200, LLC · Class II
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SKATER™ Mini-Loop Drainage Set — Argon Medical Devices, Inc. · Class I
Drainage Tube and Accessories — Hangzhou Fushan Medical Appliances Co., Ltd. · Class IIa
Exodus — NAVILYST MEDICAL, INC. · 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: Cardinalhealth

Sources (1)

FDA UDI 4d581085-3d9a-4aa5-8292-36bb14492d3c 36 fields · synced Jun 6, 2026