Catalog Number

-

Brand Name

BIOPROTECH INC.

Version/Model Number

DEEG-A-10

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

K153019,K153019,K153019

Product Code

GXY

Product Code Name

Electrode, Cutaneous

Public Device Record Key

144e4b48-89a9-49b8-95af-08086b1d5633

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

October 18, 2016

Package DI Number

28809083941004

Quantity per Package

10

Contains DI Package

18809083941007

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Master Case