Catalog Number

8939PG2

Brand Name

SharpSafety

Version/Model Number

8939PG2

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

MMK

Product Code Name

Container, sharps

Public Device Record Key

f329f063-3520-484f-99fd-626e0b65bfec

Public Version Date

March 24, 2022

Public Version Number

8

DI Record Publish Date

September 24, 2016

Package DI Number

20884521022932

Quantity per Package

5

Contains DI Package

40884521022936

Package Discontinue Date

March 23, 2022

Package Status

Not in Commercial Distribution

Package Type

CASE