Catalog Number

0792720

Brand Name

Hospira

Version/Model Number

792720

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

-

Product Code

KPE

Product Code Name

CONTAINER, I.V.

Public Device Record Key

0e1067b4-657d-4100-92aa-42da18586932

Public Version Date

October 23, 2019

Public Version Number

3

DI Record Publish Date

September 01, 2016

Package DI Number

20887787006531

Quantity per Package

24

Contains DI Package

10887787006534

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case