Catalog Number

-

Brand Name

Nunc™ Universal™ Tube, 1.8mL externally-threaded, 1D and 2D

Version/Model Number

374502NOV

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

687a2f76-bd09-4105-98f4-b7e19f1aa1ba

Public Version Date

August 02, 2022

Public Version Number

1

DI Record Publish Date

July 25, 2022

Package DI Number

30850016058530

Quantity per Package

480

Contains DI Package

10850016058536

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case