Catalog Number

DYNJP2320

Brand Name

Medline

Version/Model Number

DYNJP2320

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

MMP

Product Code Name

Cover, barrier, protective

Public Device Record Key

6d792303-a32a-4e8e-82d1-f59811471982

Public Version Date

November 18, 2020

Public Version Number

1

DI Record Publish Date

November 10, 2020

Package DI Number

40080196748045

Quantity per Package

22

Contains DI Package

10080196748044

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE