Catalog Number

-

Brand Name

Jet Port Plus

Version/Model Number

611.363.3077-HA

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

K072481,K072481

Product Code

LJT

Product Code Name

Port & Catheter, Implanted, Subcutaneous, Intravascular

Public Device Record Key

bc03e1de-be2f-41b6-9ac6-4a3ab52184f7

Public Version Date

March 06, 2020

Public Version Number

1

DI Record Publish Date

February 27, 2020

Package DI Number

07640110981917

Quantity per Package

20

Contains DI Package

07640110985489

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box