← Back to catalogue

Argyle

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Argyle FDA UDI
Generic Name
Multi-purpose percutaneous abdominothoracic drainage catheter FDA UDI
Device Name
Thoracic Catheter,Right Angle FDA UDI
Model / Reference
8888571059 FDA UDI
Description
Thoracic Catheter,Right Angle FDA UDI

Identifiers

Catalog Number
8888571059 FDA UDI
Primary DI / UDI-DI
10884521050921 FDA UDI
FDA Product Code
JOL FDA UDI
GMDN Term
Multi-purpose percutaneous abdominothoracic drainage catheter 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

Yes

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

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

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 — 32 French FDA UDI
Length — 20 Inch FDA UDI

Category: Multi-purpose percutaneous abdominothoracic drainage catheter

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

Similar devices

Also classified as Multi-purpose percutaneous abdominothoracic drainage catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 4b8140eb-4b83-4fdd-9332-18530564d02d 37 fields · synced May 31, 2026