Catalog Number

-

Brand Name

Monitor System, Patient Display

Version/Model Number

43T2564

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

HCC

Product Code Name

Device, Biofeedback

Public Device Record Key

a4d3d3b2-e88e-494d-9f3f-1765010e62f8

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

January 09, 2017

Package DI Number

10851607003126

Quantity per Package

5

Contains DI Package

00851607003129

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Shipper