Catalog Number

-

Brand Name

Nunc™ Universal™ Tube, 2 mL internally-threaded, Coded-rack

Version/Model Number

374510-BR

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

-

Product Code

FMH

Product Code Name

CONTAINER, SPECIMEN, STERILE

Public Device Record Key

35f8d1a6-5bc1-42fa-9a49-709ef523ad17

Public Version Date

June 21, 2022

Public Version Number

1

DI Record Publish Date

June 11, 2022

Package DI Number

30850016058561

Quantity per Package

10

Contains DI Package

10850016058567

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case