Catalog Number

-

Brand Name

McKesson

Version/Model Number

16-1316

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

LRY

Product Code Name

Punch, Surgical

Public Device Record Key

2ccc0e6e-3c76-43f5-bad3-3ba621547ff9

Public Version Date

July 28, 2020

Public Version Number

1

DI Record Publish Date

July 20, 2020

Package DI Number

00612479255982

Quantity per Package

25

Contains DI Package

00612479255975

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box