Catalog Number

-

Brand Name

Drive

Version/Model Number

22330

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"

-

For Single-Use

-

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

3726eafe-2f22-4e8f-9a1f-d7b655ab7f48

Public Version Date

December 01, 2021

Public Version Number

11

DI Record Publish Date

September 16, 2016

Package DI Number

50822383294877

Quantity per Package

6

Contains DI Package

00822383294872

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-