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Salem Sump

FDA UDI

Class II (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
Salem Sump FDA UDI
Generic Name
Gastrostomy tube FDA UDI
Device Name
Infant Feeding Tube FDA UDI
Model / Reference
5558260807 FDA UDI
Description
Infant Feeding Tube FDA UDI

Identifiers

Catalog Number
5558260807 FDA UDI
Primary DI / UDI-DI
50192253038703 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Gastrostomy 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

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Gastrostomy tube

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

Similar devices

Also classified as Gastrostomy tube.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1f718ec4-ad94-461f-92d8-0f52cf460c68 34 fields · synced Jun 6, 2026