Catalog Number

33

Brand Name

UE BioSleeve

Version/Model Number

5

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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

K141342,K141342

Product Code

GXY

Product Code Name

Electrode, Cutaneous

Public Device Record Key

527226de-55cf-48cf-b172-9e585861af7b

Public Version Date

February 19, 2021

Public Version Number

2

DI Record Publish Date

January 08, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-