Catalog Number

-

Brand Name

MEDICAL ACTION INDUSTRIES

Version/Model Number

78716

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)

Yes

Over the Counter (OTC)

-

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

ad94ea37-4768-40a8-9f31-24591e478ea4

Public Version Date

August 21, 2019

Public Version Number

2

DI Record Publish Date

October 11, 2018

Package DI Number

20809160213374

Quantity per Package

20

Contains DI Package

10809160213377

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-