Catalog Number

-

Brand Name

McKesson

Version/Model Number

16-N6100

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

GAZ

Product Code Name

Tubing, Noninvasive

Public Device Record Key

ec3a0b42-0fc6-4772-87b3-221e56ea57ea

Public Version Date

June 08, 2021

Public Version Number

5

DI Record Publish Date

December 09, 2016

Package DI Number

40612479184761

Quantity per Package

100

Contains DI Package

20612479185429

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case