Catalog Number

014.01

Brand Name

V. Mueller

Version/Model Number

014.01

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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

FQM

Product Code Name

BANDAGE, ELASTIC

Public Device Record Key

8f568615-40ed-4931-8647-f1e514b4fec7

Public Version Date

August 13, 2018

Public Version Number

1

DI Record Publish Date

July 12, 2018

Package DI Number

20885403160438

Quantity per Package

15

Contains DI Package

10885403160431

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box