Catalog Number

-

Brand Name

Medical Action Industries

Version/Model Number

76769

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

f63e7d64-180e-4a32-b4f6-bd3d67d7e1ba

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

December 27, 2016

Package DI Number

20809160118228

Quantity per Package

20

Contains DI Package

10809160118221

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-