Catalog Number

DYNJGWIRE02

Brand Name

Medline Industries, Inc.

Version/Model Number

DYNJGWIRE02

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

-

Product Code

DQO

Product Code Name

Catheter, intravascular, diagnostic

Public Device Record Key

00025acd-529c-49b3-9203-e0f776e1667a

Public Version Date

August 02, 2022

Public Version Number

7

DI Record Publish Date

September 29, 2016

Package DI Number

40884389849980

Quantity per Package

10

Contains DI Package

10884389849989

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE