Catalog Number

502

Brand Name

Leg and Arm Cast Elevators

Version/Model Number

502

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

CCX

Product Code Name

Support, Patient Position

Public Device Record Key

d629f7bf-e5d4-4ae6-98e0-ef549a9fa108

Public Version Date

July 15, 2020

Public Version Number

2

DI Record Publish Date

February 24, 2020

Package DI Number

00810044960020

Quantity per Package

3

Contains DI Package

10810044960027

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case