Catalog Number

-

Brand Name

A&E Medical / Rotating Surgical Punches

Version/Model Number

080-453

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"

-

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

14819887-e74f-4aeb-9a00-6864a945df9a

Public Version Date

July 17, 2019

Public Version Number

1

DI Record Publish Date

July 09, 2019

Package DI Number

20841291106972

Quantity per Package

6

Contains DI Package

10841291106975

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-