Catalog Number

-

Brand Name

Drive

Version/Model Number

13019

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FSA

Product Code Name

LIFT, PATIENT, NON-AC-POWERED

Public Device Record Key

cf5faa93-81ce-4530-8d83-7ce701020169

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

May 19, 2017

Package DI Number

50822383103254

Quantity per Package

50

Contains DI Package

00822383103259

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-