Curity - True content to be populated as part of rebranding - Cardinal Health, Inc.

Duns Number:080935429

Device Description: True content to be populated as part of rebranding

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More Product Details

Catalog Number

2259G

Brand Name

Curity

Version/Model Number

2259G

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

FRL

Product Code Name

FIBER, MEDICAL, ABSORBENT

Device Record Status

Public Device Record Key

fd4fcff8-4c20-45a5-86d8-64cb30f9cf9f

Public Version Date

August 24, 2021

Public Version Number

2

DI Record Publish Date

November 14, 2019

Additional Identifiers

Package DI Number

50885380174504

Quantity per Package

20

Contains DI Package

30885380174500

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