Catalog Number

-

Brand Name

Custom Healthcare Systems Inc.

Version/Model Number

D8-16156

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

KJG

Product Code Name

Tube, Tissue Culture

Public Device Record Key

73a0db9e-1043-4ace-bc62-5390225b1f46

Public Version Date

February 05, 2021

Public Version Number

2

DI Record Publish Date

July 26, 2018

Package DI Number

20811870030394

Quantity per Package

100

Contains DI Package

00811870030390

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

N/A