Catalog Number

-

Brand Name

GS27

Version/Model Number

BMI GS27

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K101576

Product Code

DRX

Product Code Name

Electrode, Electrocardiograph

Public Device Record Key

bcd6ddaf-2c6d-4283-8eea-f3f4edea6365

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

November 30, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-