Catalog Number

-

Brand Name

Plasti-Products

Version/Model Number

149154

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

-

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

b203bd2e-ace8-425e-91b8-3e3e9e019971

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

April 15, 2016

Package DI Number

40797876191540

Quantity per Package

2

Contains DI Package

10797876191549

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case