Catalog Number

-

Brand Name

McKesson

Version/Model Number

240P

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

MCZ

Product Code Name

Suture Removal Kit

Public Device Record Key

c31410b0-0a13-482b-9d50-539e7a79093f

Public Version Date

July 03, 2020

Public Version Number

1

DI Record Publish Date

June 25, 2020

Package DI Number

40612479205947

Quantity per Package

50

Contains DI Package

10612479205939

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case