Catalog Number

412-557

Brand Name

MCKENTY ELEVATOR

Version/Model Number

412-557

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

-

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

HTE

Product Code Name

Elevator

Public Device Record Key

3b3645f3-3dcd-4ed8-8fe8-2f8f8ab5bec2

Public Version Date

December 04, 2020

Public Version Number

2

DI Record Publish Date

September 04, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-