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Argyle

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Argyle FDA UDI
Generic Name
Blood/tissue storage/culture container FDA UDI
Device Name
Two Bottle Drainage System,9/32 inch (0.7 cm) Tubing FDA UDI
Model / Reference
8884726200 FDA UDI
Description
Two Bottle Drainage System,9/32 inch (0.7 cm) Tubing FDA UDI

Identifiers

Catalog Number
8884726200 FDA UDI
Primary DI / UDI-DI
30884521118298 FDA UDI
FDA Product Code
KDQ FDA UDI
GMDN Term
Blood/tissue storage/culture container 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

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

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
Outer Diameter — 0.28125 Inch FDA UDI
Total Volume — 2000 Milliliter FDA UDI

Category: Blood/tissue storage/culture container

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

Similar devices

Also classified as Blood/tissue storage/culture container.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 2cd8c123-7ffe-40d1-9f06-62c5ecc7734a 37 fields · synced Jun 8, 2026