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Argyle

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Argyle FDA UDI
Generic Name
Non-ISO80369-standardized small-bore multichannel connector, reusable FDA UDI
Device Name
Suction Tubing,Integral Funnel/Funnel, Non-Conductive FDA UDI
Model / Reference
5558301734 FDA UDI
Description
Suction Tubing,Integral Funnel/Funnel, Non-Conductive FDA UDI

Identifiers

Catalog Number
5558301734 FDA UDI
Primary DI / UDI-DI
10884527019328 FDA UDI
FDA Product Code
GAZ FDA UDI
GMDN Term
Non-ISO80369-standardized small-bore multichannel connector, reusable 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 0.28125 Inch FDA UDI
Length — 20 Feet FDA UDI

Category: Non-ISO80369-standardized small-bore multichannel connector, reusable

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

Similar devices

Also classified as Non-ISO80369-standardized small-bore multichannel connector, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI a4a7e838-ae86-40d3-9e20-f6e1669cc80f 37 fields · synced Jun 1, 2026