Catalog Number

331320

Brand Name

Dri-Aids

Version/Model Number

331320

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

KHR

Product Code Name

ABSORBER, SALIVA, PAPER

Public Device Record Key

45baaa7d-4c8e-431e-b61d-03df7227af4e

Public Version Date

October 05, 2022

Public Version Number

5

DI Record Publish Date

December 08, 2020

Package DI Number

20789594000644

Quantity per Package

13

Contains DI Package

10789594000647

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case