Catalog Number

-

Brand Name

STARLET COMPL. WITH ACCESS.

Version/Model Number

185082

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

JQW

Product Code Name

Station, Pipetting And Diluting, For Clinical Use

Public Device Record Key

804f8bc2-5f69-4e4d-b107-fee8555041bb

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

December 03, 2014

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-