Catalog Number

-

Brand Name

IV ADMINISTRATION SET B400 SP

Version/Model Number

MC72DC

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

October 29, 2018

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

-

Product Code

FPA

Product Code Name

Set, administration, intravascular

Public Device Record Key

b1583b53-5bf7-45b5-8c9d-93eee17876a9

Public Version Date

April 07, 2021

Public Version Number

6

DI Record Publish Date

October 21, 2016

Package DI Number

50884908029838

Quantity per Package

25

Contains DI Package

00884908029833

Package Discontinue Date

October 29, 2018

Package Status

Not in Commercial Distribution

Package Type

box