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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
Suction system catheter, general-purpose FDA UDI
Device Name
Argyle Flexible Yankauer Fine Capacity 12 Fr/Ch (4.0 mm) x 25 cm FDA UDI
Model / Reference
8888504001 FDA UDI
Description
Argyle Flexible Yankauer Fine Capacity 12 Fr/Ch (4.0 mm) x 25 cm FDA UDI

Identifiers

Catalog Number
8888504001 FDA UDI
Primary DI / UDI-DI
10192253041583 FDA UDI
FDA Product Code
GCX FDA UDI
GMDN Term
Suction system catheter, general-purpose 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Suction system catheter, general-purpose

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

Similar devices

Also classified as Suction system catheter, general-purpose.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c9550dd4-944e-47fd-86df-fcdd4100c7fd 34 fields · synced Jun 8, 2026