Catalog Number

-

Brand Name

STERiGLIDE TM

Version/Model Number

SGC-25038

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

5f72c7e0-55ef-4a68-9fc1-03f13a3af187

Public Version Date

July 28, 2022

Public Version Number

2

DI Record Publish Date

April 07, 2022

Package DI Number

14580708061730

Quantity per Package

2

Contains DI Package

04580708061733

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-