CARDINAL HEALTH - STETHOSCOPE ADULT DUAL HEAD BLACK - Cardinal Health 200, LLC

Duns Number:961027315

Device Description: STETHOSCOPE ADULT DUAL HEAD BLACK

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More Product Details

Catalog Number

SMD21ABK

Brand Name

CARDINAL HEALTH

Version/Model Number

SMD21ABK

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

-

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

LDE

Product Code Name

STETHOSCOPE, MANUAL

Device Record Status

Public Device Record Key

107505ce-9a55-4833-8104-138cff0b1dd0

Public Version Date

June 14, 2019

Public Version Number

1

DI Record Publish Date

June 06, 2019

Additional Identifiers

Package DI Number

20888499002002

Quantity per Package

10

Contains DI Package

10888499002005

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