Catalog Number

-

Brand Name

Medical Action Industries

Version/Model Number

81536

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"

Yes

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

Yes

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

-

FDA Premarket Submission

-

Product Code

OIE

Product Code Name

Urine collection kit (excludes HIV testing)

Public Device Record Key

c300c37b-faf5-42ad-b867-5905448914e1

Public Version Date

September 07, 2020

Public Version Number

1

DI Record Publish Date

August 28, 2020

Package DI Number

20809160290726

Quantity per Package

20

Contains DI Package

10809160290729

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-