Catalog Number

-

Brand Name

MediChoice

Version/Model Number

DP0300

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

LRY

Product Code Name

PUNCH, SURGICAL

Public Device Record Key

0fadc50c-ec9c-4235-b5c6-6d8d9a27ff23

Public Version Date

November 02, 2020

Public Version Number

1

DI Record Publish Date

October 23, 2020

Package DI Number

50885632109667

Quantity per Package

25

Contains DI Package

10885632109669

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-