Catalog Number

31140372

Brand Name

Devon

Version/Model Number

31140372

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

MDM

Product Code Name

INSTRUMENT, MANUAL, SURGICAL, GENERAL USE

Public Device Record Key

a454c5d8-915d-4db9-8ac9-844d58676180

Public Version Date

June 05, 2020

Public Version Number

3

DI Record Publish Date

June 23, 2018

Package DI Number

10884527018796

Quantity per Package

40

Contains DI Package

20884527018793

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE