Catalog Number

-

Brand Name

Medical Action Industries

Version/Model Number

56273

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

October 19, 2021

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

4f761a36-ec81-45da-8f84-9d44b1c61664

Public Version Date

October 21, 2021

Public Version Number

4

DI Record Publish Date

August 20, 2016

Package DI Number

20809160003821

Quantity per Package

20

Contains DI Package

10809160003824

Package Discontinue Date

October 19, 2021

Package Status

Not in Commercial Distribution

Package Type

-