Catalog Number

1000SC2 01; 1000SC2 10

Brand Name

Bemis

Version/Model Number

1000SC2

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

8ab1cbcd-10e8-4ae1-b46f-bdbe9e937d14

Public Version Date

April 12, 2022

Public Version Number

1

DI Record Publish Date

April 04, 2022

Package DI Number

20073088148661

Quantity per Package

10

Contains DI Package

00073088148667

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton