Catalog Number

3000SC 01; 3000SC 10

Brand Name

Bemis

Version/Model Number

3000SC

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

KDQ

Product Code Name

Bottle, Collection, Vacuum

Public Device Record Key

8117f114-3d90-40d1-9307-244e0915e760

Public Version Date

January 08, 2021

Public Version Number

4

DI Record Publish Date

September 24, 2016

Package DI Number

20073088149453

Quantity per Package

10

Contains DI Package

00073088149459

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton