← Back to catalogue

Argyle

FDA UDI

Class I (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Argyle FDA UDI
Generic Name
Low-pressure tubing connector, reusable FDA UDI
Device Name
Female Luer-Lock Connector,Polypropylene FDA UDI
Model / Reference
5558275003 FDA UDI
Description
Female Luer-Lock Connector,Polypropylene FDA UDI

Identifiers

Catalog Number
5558275003 FDA UDI
Primary DI / UDI-DI
10884521151253 FDA UDI
FDA Product Code
GCD FDA UDI
GMDN Term
Low-pressure tubing connector, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 140 Milliliter FDA UDI

Category: Low-pressure tubing connector, reusable

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

Similar devices

Also classified as Low-pressure tubing connector, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 0dfd6451-b813-4173-bc6e-4b7755503e22 37 fields · synced Jun 8, 2026