Catalog Number

-

Brand Name

DRIVEMEDICAL

Version/Model Number

18304GN

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

CAN

Product Code Name

REGULATOR, PRESSURE, GAS CYLINDER

Public Device Record Key

a34b8fdb-9a01-4fa4-b2da-4a4b8d8278dd

Public Version Date

July 07, 2020

Public Version Number

2

DI Record Publish Date

June 21, 2019

Package DI Number

50822383283246

Quantity per Package

20

Contains DI Package

00822383283241

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-