Catalog Number

SleeveL

Brand Name

Protech Proguard

Version/Model Number

SleeveL

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)

Yes

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

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

KPY

Product Code Name

Shield, Protective, Personnel

Public Device Record Key

6170818d-bbaf-42c0-a753-7d24c735e9c9

Public Version Date

April 16, 2018

Public Version Number

1

DI Record Publish Date

March 15, 2018

Package DI Number

08054301890961

Quantity per Package

3

Contains DI Package

08054301890220

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-