Catalog Number

-

Brand Name

Medical Action Industries

Version/Model Number

73733B

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

November 16, 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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

NWU

Product Code Name

Endoscope introducer kit

Public Device Record Key

1c6cf1bb-de99-42d2-8994-ec9316f84821

Public Version Date

November 17, 2020

Public Version Number

4

DI Record Publish Date

April 21, 2017

Package DI Number

20809160145460

Quantity per Package

20

Contains DI Package

10809160145463

Package Discontinue Date

November 16, 2020

Package Status

Not in Commercial Distribution

Package Type

-