Catalog Number

-

Brand Name

McKesson

Version/Model Number

26556

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

FMI

Product Code Name

Needle, Hypodermic, Single Lumen

Public Device Record Key

21705c50-f220-487e-baec-a41091f8d567

Public Version Date

October 23, 2019

Public Version Number

6

DI Record Publish Date

December 09, 2016

Package DI Number

20612479201334

Quantity per Package

50

Contains DI Package

10612479201320

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box