Catalog Number

-

Brand Name

Globe Scientific

Version/Model Number

3895

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

NNI

Product Code Name

Container, Specimen, Non-Sterile

Public Device Record Key

f6c62333-c348-4a7b-8f8c-d1e9488f5861

Public Version Date

December 04, 2019

Public Version Number

1

DI Record Publish Date

November 26, 2019

Package DI Number

00840095606264

Quantity per Package

30

Contains DI Package

00840095606271

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case