Catalog Number

8851NB

Brand Name

Kendall

Version/Model Number

8851NB

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

March 01, 2021

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FMI

Product Code Name

Needle, hypodermic, single lumen

Public Device Record Key

4a669064-2bd0-4c8f-b4dc-794400c4a7c9

Public Version Date

March 01, 2021

Public Version Number

9

DI Record Publish Date

September 24, 2016

Package DI Number

10884521141629

Quantity per Package

10

Contains DI Package

20884521141626

Package Discontinue Date

March 01, 2021

Package Status

Not in Commercial Distribution

Package Type

CASE