Medline - DBD-BANDAGE,SRTSTRTCH,10CMX5M,3.94X5.47Y - MEDLINE INDUSTRIES, INC.

Duns Number:025460908

Device Description: DBD-BANDAGE,SRTSTRTCH,10CMX5M,3.94X5.47Y

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More Product Details

Catalog Number

MDS099004SSHL

Brand Name

Medline

Version/Model Number

MDS099004SSHL

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)

-

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

FQM

Product Code Name

BANDAGE, ELASTIC

Device Record Status

Public Device Record Key

20f13528-7c8d-46a3-b85d-4ff75c4ccc16

Public Version Date

September 20, 2021

Public Version Number

2

DI Record Publish Date

January 20, 2021

Additional Identifiers

Package DI Number

20888277702285

Quantity per Package

20

Contains DI Package

10888277702288

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE

"MEDLINE INDUSTRIES, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 38540
2 A medical device with a moderate to high risk that requires special controls. 85094
3 A medical device with high risk that requires premarket approval 2
U Unclassified 7