Catalog Number

-

Brand Name

UNBRANDED

Version/Model Number

104NS

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

KPE

Product Code Name

CONTAINER, I.V.

Public Device Record Key

79e9726c-9be4-41c0-8e58-7e51a347224e

Public Version Date

February 19, 2021

Public Version Number

3

DI Record Publish Date

September 19, 2016

Package DI Number

10848340005203

Quantity per Package

100

Contains DI Package

00848340005206

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-