Catalog Number

1000NP

Brand Name

Kendall

Version/Model Number

1000NP

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

January 01, 2023

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"

-

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

c3ef1588-f505-4469-b3a1-791104f11c79

Public Version Date

January 12, 2022

Public Version Number

10

DI Record Publish Date

September 24, 2016

Package DI Number

10884521184343

Quantity per Package

120

Contains DI Package

10884521537422

Package Discontinue Date

January 01, 2023

Package Status

In Commercial Distribution

Package Type

CASE