Catalog Number

-

Brand Name

Medical Action Industries

Version/Model Number

81234

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

KDC

Product Code Name

INSTRUMENT, SURGICAL, DISPOSABLE

Public Device Record Key

98de8933-634c-4d3a-909d-60c482c50ee1

Public Version Date

September 23, 2022

Public Version Number

2

DI Record Publish Date

February 07, 2020

Package DI Number

20809160277871

Quantity per Package

50

Contains DI Package

10809160277874

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-