Catalog Number

32-1331

Brand Name

DeRoyal

Version/Model Number

32-1331

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)

Yes

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

FMH

Product Code Name

CONTAINER, SPECIMEN, STERILE

Public Device Record Key

6fe32011-304a-4a9f-8555-60e6eb0fd603

Public Version Date

July 22, 2021

Public Version Number

2

DI Record Publish Date

June 30, 2021

Package DI Number

50749756115570

Quantity per Package

100

Contains DI Package

00749756115575

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case