3M™ Littmann® Cardiology IV™ - 3M™ Littmann® Cardiology IV™ Diagnostic - 3M COMPANY

Duns Number:830016148

Device Description: 3M™ Littmann® Cardiology IV™ Diagnostic Stethoscope, 6151, Standard-Finish Chestpiece, Bla 3M™ Littmann® Cardiology IV™ Diagnostic Stethoscope, 6151, Standard-Finish Chestpiece, Black Tube, Stainless Stem

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More Product Details

Catalog Number

6151

Brand Name

3M™ Littmann® Cardiology IV™

Version/Model Number

6151

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

79ac6ef4-fa59-43c1-b5e0-5b64ef315ea8

Public Version Date

August 24, 2021

Public Version Number

1

DI Record Publish Date

August 16, 2021

Additional Identifiers

Package DI Number

50707387789768

Quantity per Package

3

Contains DI Package

00707387789763

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX

"3M COMPANY" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 274
2 A medical device with a moderate to high risk that requires special controls. 444
U Unclassified 7