Catalog Number

-

Brand Name

STORM Sterile Operating Kit

Version/Model Number

1-10-10

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"

-

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

-

Product Code

HTY

Product Code Name

Pin, Fixation, Smooth

Public Device Record Key

a64a6451-66ea-46ea-a6dc-eef0c34e2887

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 23, 2016

Package DI Number

5060309870020

Quantity per Package

5

Contains DI Package

05060309870013

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton