Catalog Number

150 030

Brand Name

BEMIS

Version/Model Number

150 030

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

July 30, 2022

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

K931664,K931664

Product Code

MMK

Product Code Name

Container, Sharps

Public Device Record Key

f4fa365a-30aa-4c6d-aacb-b62151caa548

Public Version Date

August 05, 2022

Public Version Number

4

DI Record Publish Date

September 24, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-