Catalog Number

-

Brand Name

903™

Version/Model Number

105

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

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

JKA

Product Code Name

Tubes, Vials, Systems, Serum Separators, Blood Collection

Public Device Record Key

99cf3028-acfe-419c-a8e8-09f7467d9cd1

Public Version Date

December 06, 2018

Public Version Number

2

DI Record Publish Date

September 14, 2018

Package DI Number

00860802000338

Quantity per Package

7200

Contains DI Package

00860802000321

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-