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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
Oropharyngeal secretion specimen suction kit FDA UDI
Device Name
Argyle Graduated Suction Catheter Tray with Chimney Valve 8 Fr/Ch FDA UDI
Model / Reference
10082 FDA UDI
Description
Argyle Graduated Suction Catheter Tray with Chimney Valve 8 Fr/Ch FDA UDI

Identifiers

Catalog Number
10082 FDA UDI
Primary DI / UDI-DI
10192253041613 FDA UDI
FDA Product Code
JOL FDA UDI
GMDN Term
Oropharyngeal secretion specimen suction kit 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

Yes

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: Oropharyngeal secretion specimen suction kit

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

Similar devices

Also classified as Oropharyngeal secretion specimen suction kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinal Health 200, LLC

Sources (1)

  • FDA UDI 3f2a4f9f-aa1f-4b7b-96c5-7518dacaccb3 35 fields · synced Jun 8, 2026