Catalog Number

-

Brand Name

McKesson

Version/Model Number

16-43445-01

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

-

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

KDQ

Product Code Name

Bottle, Collection, Vacuum

Public Device Record Key

737cf06d-a8f7-48cc-b22d-ce9dbba474e2

Public Version Date

January 08, 2021

Public Version Number

3

DI Record Publish Date

June 24, 2019

Package DI Number

40612479243208

Quantity per Package

10

Contains DI Package

10612479243191

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case