Catalog Number

-

Brand Name

Centrifuge Tube 50 mL

Version/Model Number

16106

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

PUD

Product Code Name

Labware, Assisted Reproduction, Exempt

Public Device Record Key

b6397117-b512-4954-a4c7-186a1b77f127

Public Version Date

June 08, 2020

Public Version Number

1

DI Record Publish Date

May 29, 2020

Package DI Number

27350025914606

Quantity per Package

12

Contains DI Package

17350025914609

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-