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Argyle

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Argyle FDA UDI
Generic Name
Gastric lavage system FDA UDI
Device Name
Pediatric Edlich Gastric Lavage Tray,Medium FDA UDI
Model / Reference
8888750513 FDA UDI
Description
Pediatric Edlich Gastric Lavage Tray,Medium FDA UDI

Identifiers

Catalog Number
8888750513 FDA UDI
Primary DI / UDI-DI
10884521000735 FDA UDI
FDA Product Code
KDH FDA UDI
GMDN Term
Gastric lavage system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5980 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

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

No

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
Length — 36 Inch FDA UDI
Catheter Gauge — 24 French FDA UDI

Category: Gastric lavage system

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

Similar devices

Also classified as Gastric lavage system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI db2c6dd0-185e-47bb-ae6e-f936dfe52f16 37 fields · synced May 31, 2026