Catalog Number

-

Brand Name

STERiGLIDE TM

Version/Model Number

SGA-050038A

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

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

GEA

Product Code Name

CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY

Public Device Record Key

f81fef1a-f7aa-4967-9213-373bd5989af6

Public Version Date

March 02, 2020

Public Version Number

1

DI Record Publish Date

February 21, 2020

Package DI Number

14571225317271

Quantity per Package

192

Contains DI Package

04571225317274

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-