Catalog Number

-

Brand Name

Drive

Version/Model Number

412100200

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

FSA

Product Code Name

LIFT, PATIENT, NON-AC-POWERED

Public Device Record Key

01315b24-c9c9-4033-be33-121c96ff5612

Public Version Date

July 01, 2019

Public Version Number

1

DI Record Publish Date

June 21, 2019

Package DI Number

50822383259975

Quantity per Package

10

Contains DI Package

00822383259970

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-