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Cardinal Health

FDA UDI

Class II (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
CARDINAL HEALTH FDA UDI
Generic Name
Nasogastric/orogastric tube FDA UDI
Device Name
Salem Sump Dual Lumen Stomach Tube with ENFit Connection FDA UDI
Model / Reference
8888266130E FDA UDI
Description
Salem Sump Dual Lumen Stomach Tube with ENFit Connection FDA UDI

Identifiers

Catalog Number
8888266130E FDA UDI
Primary DI / UDI-DI
10192253012835 FDA UDI
FDA Product Code
FEG FDA UDI
PIF FDA UDI
GMDN Term
Nasogastric/orogastric tube 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Catheter Gauge — 16 French FDA UDI
Length — 48 Inch FDA UDI

Category: Nasogastric/orogastric tube

Cardinal Health by Cardinal Health 200, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasogastric/orogastric tube.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinal Health 200, LLC

Sources (1)

  • FDA UDI ed9fd2da-8c3a-4a1d-ba23-db388a6cc0c2 35 fields · synced Jun 8, 2026