Catalog Number

-

Brand Name

Moore Medical

Version/Model Number

23500

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

-

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

GEH

Product Code Name

Unit, Cryosurgical, Accessories

Public Device Record Key

0f065105-20ca-4aed-9d94-b7480f0b999e

Public Version Date

April 07, 2021

Public Version Number

3

DI Record Publish Date

December 09, 2016

Package DI Number

40607415001769

Quantity per Package

1

Contains DI Package

10607415001751

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case