Catalog Number

4154108

Brand Name

BARD Poly Midline

Version/Model Number

4154108

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

Yes

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

-

FDA Premarket Submission

-

Product Code

LJS

Product Code Name

Catheter,intravascular,therapeutic,long-term greater than 30 days

Public Device Record Key

4df9d8a8-3dec-4d7e-9b1f-939b46ab2c74

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 23, 2015

Package DI Number

10801741037655

Quantity per Package

5

Contains DI Package

00801741037658

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CA