Catalog Number

-

Brand Name

Medical Action Industries

Version/Model Number

75295

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

March 19, 2020

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

CAZ

Product Code Name

Anesthesia conduction kit

Public Device Record Key

6fe6be5e-bd48-4cb0-b4e1-98153afdc577

Public Version Date

March 20, 2020

Public Version Number

3

DI Record Publish Date

August 20, 2016

Package DI Number

20809160021092

Quantity per Package

20

Contains DI Package

10809160021095

Package Discontinue Date

March 19, 2020

Package Status

Not in Commercial Distribution

Package Type

-