CARDINAL HEALTH - DRIVELINE MGMT ANCHOR DAILY XL - Cardinal Health 200, LLC

Duns Number:961027315

Device Description: DRIVELINE MGMT ANCHOR DAILY XL

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More Product Details

Catalog Number

03A5689C

Brand Name

CARDINAL HEALTH

Version/Model Number

03A5689C

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"

Yes

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

OXQ

Product Code Name

Dressing change tray

Device Record Status

Public Device Record Key

7117bdcf-3506-423d-a321-e1a54e825b33

Public Version Date

June 17, 2022

Public Version Number

3

DI Record Publish Date

February 25, 2019

Additional Identifiers

Package DI Number

50888439315736

Quantity per Package

30

Contains DI Package

10888439315738

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE

"CARDINAL HEALTH 200, LLC" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 101686
2 A medical device with a moderate to high risk that requires special controls. 139430
3 A medical device with high risk that requires premarket approval 8
U Unclassified 40