Catalog Number

100ECO 030

Brand Name

BEMIS

Version/Model Number

100ECO 030

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

January 29, 2020

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

K960525,K960525

Product Code

MMK

Product Code Name

Container, Sharps

Public Device Record Key

09ec5b59-d8b0-4a97-953e-82059164a30b

Public Version Date

January 30, 2020

Public Version Number

4

DI Record Publish Date

December 02, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-