Catalog Number

-

Brand Name

Medical Systems

Version/Model Number

901100

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

LHI

Product Code Name

Set, I.V. Fluid Transfer

Public Device Record Key

f8d3dde3-c795-42ee-9d9f-1b584bc5065d

Public Version Date

April 07, 2021

Public Version Number

4

DI Record Publish Date

September 24, 2016

Package DI Number

813153024027

Quantity per Package

1

Contains DI Package

10813153024024

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-