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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
Arygle Suction Catheter with Chimney Valve Striaght Packed 10 Fr/ Ch FDA UDI
Model / Reference
31000 FDA UDI
Description
Arygle Suction Catheter with Chimney Valve Striaght Packed 10 Fr/ Ch FDA UDI

Identifiers

Catalog Number
31000- FDA UDI
Primary DI / UDI-DI
10192253041989 FDA UDI
FDA Product Code
JOL 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

Yes

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

Dimensions & Sizes

Size
Catheter Gauge — 10 French 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 69e6f2f2-c3c7-4240-8c57-8ebe6b750f3b 35 fields · synced Jun 8, 2026