Catalog Number

123110

Brand Name

EAMIS Lite™

Version/Model Number

EA-RAIL

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K142420

Product Code

IYE

Product Code Name

Accelerator, Linear, Medical

Public Device Record Key

5a37a93f-08b0-4439-9c7a-2c21d0194500

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

April 03, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-