Catalog Number

-

Brand Name

3CP™ Centrifuge Kit

Version/Model Number

1

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

BK170002

Product Code

PMQ

Product Code Name

Peripheral Blood Processing Device For Wound Management

Public Device Record Key

ed2c734a-12dc-45de-8250-e3da2b7cfa2a

Public Version Date

June 10, 2022

Public Version Number

2

DI Record Publish Date

July 19, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-