Catalog Number

DYNJ901920D

Brand Name

Medline Industries, Inc.

Version/Model Number

DYNJ901920D

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"

-

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

K900129

Product Code

GDW

Product Code Name

STAPLE, IMPLANTABLE

Public Device Record Key

200e582a-1f33-4e2d-8dd4-aa0560f46eb5

Public Version Date

June 17, 2022

Public Version Number

5

DI Record Publish Date

August 28, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-