Salem Sump - Salem Sump Dual Lumen Stomach Tubewith ENFit - Cardinal Health, Inc.

Duns Number:080935429

Device Description: Salem Sump Dual Lumen Stomach Tubewith ENFit Connection

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More Product Details

Catalog Number

8888264929E

Brand Name

Salem Sump

Version/Model Number

8888264929E

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code Details

Product Code

FEG

Product Code Name

TUBE, DOUBLE LUMEN FOR INTESTINAL DECOMPRESSION AND/OR INTUBATION

Device Record Status

Public Device Record Key

42ecd40f-405a-454e-903c-e82c1387f121

Public Version Date

January 24, 2022

Public Version Number

1

DI Record Publish Date

January 14, 2022

Additional Identifiers

Package DI Number

20884521779423

Quantity per Package

50

Contains DI Package

10884521779426

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE

"CARDINAL HEALTH, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 672
2 A medical device with a moderate to high risk that requires special controls. 1692
U Unclassified 17