Catalog Number

-

Brand Name

Medical Action Industries

Version/Model Number

56455

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

3f6b5300-2e47-44b3-afa8-8b3da3cb8404

Public Version Date

September 23, 2022

Public Version Number

5

DI Record Publish Date

August 20, 2016

Package DI Number

20809160005559

Quantity per Package

20

Contains DI Package

10809160005552

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-