Catalog Number

AME-002500 US

Brand Name

EarlySense® Central Display Unit

Version/Model Number

N/A

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K151006

Product Code

MSX

Product Code Name

System,Network And Communication,Physiological Monitors

Public Device Record Key

67151b0e-345a-44de-ad9f-e1534514b783

Public Version Date

May 19, 2020

Public Version Number

4

DI Record Publish Date

June 16, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-