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Argyle

FDA UDI

Class II (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
Argyle FDA UDI
Generic Name
Nasoenteral tube FDA UDI
Device Name
Feeding Tube • Radiopaque FDA UDI
Model / Reference
461008 FDA UDI
Description
Feeding Tube • Radiopaque FDA UDI

Identifiers

Catalog Number
461008 FDA UDI
Primary DI / UDI-DI
10192253007763 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Nasoenteral tube FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5980 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 — 5 French FDA UDI
Length — 36 Inch FDA UDI

Category: Nasoenteral tube

Argyle by Cardinal Health 200, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasoenteral tube.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cddfb2dc-9ca4-4151-9c1c-60377d5e6c46 35 fields · synced Jun 8, 2026