Catalog Number

3000 01; 3000 10

Brand Name

Bemis

Version/Model Number

3000

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

-

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

KDQ

Product Code Name

Bottle, Collection, Vacuum

Public Device Record Key

da4db5b9-6b2a-40b9-8e5a-7286c589a448

Public Version Date

August 05, 2022

Public Version Number

6

DI Record Publish Date

September 24, 2016

Package DI Number

20073088149439

Quantity per Package

10

Contains DI Package

00073088149435

Package Discontinue Date

January 06, 2022

Package Status

Not in Commercial Distribution

Package Type

Carton