Catalog Number

-

Brand Name

A&E Medical / Rotating Surgical Punches

Version/Model Number

080-501

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

162f122f-ab01-4664-b714-64da5a093a88

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

December 01, 2016

Package DI Number

20841291105241

Quantity per Package

6

Contains DI Package

10841291105244

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-