Salem Sump

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name: Salem Sump FDA UDI
Generic Name: Sump drain FDA UDI
Device Name: Dual Lumen Stomach Tube,Anti-Reflux Valve FDA UDI
Model / Reference: 8888266114 FDA UDI
Description: Dual Lumen Stomach Tube,Anti-Reflux Valve FDA UDI

Identifiers

Catalog Number: 8888266114 FDA UDI
Primary DI / UDI-DI: 10884521004689 FDA UDI
FDA Product Code: FEG FDA UDI
GMDN Term: Sump drain 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Catheter Gauge — 12 French FDA UDI
Length — 48 Inch FDA UDI

Category: Sump drain

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

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Salem Sump — Cardinal Health 200, LLC · Class II
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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Cardinalhealth

Sources (1)

FDA UDI a48525ac-2900-43e2-81af-c4dcdcfed879 37 fields · synced Jun 8, 2026