Kerlix - Sponges,16 Ply - Cardinal Health, Inc.

Duns Number:080935429

Device Description: Sponges,16 Ply

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More Product Details

Catalog Number

5042

Brand Name

Kerlix

Version/Model Number

5042

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code Details

Product Code

NAB

Product Code Name

Gauze / sponge,nonresorbable for external use

Device Record Status

Public Device Record Key

6b6f0f73-4395-4c5e-ae52-c25e897a634c

Public Version Date

August 24, 2021

Public Version Number

3

DI Record Publish Date

June 30, 2018

Additional Identifiers

Package DI Number

20884527016874

Quantity per Package

2000

Contains DI Package

10884527016877

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