Catalog Number

31140398

Brand Name

Devon

Version/Model Number

31140398

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

ffe6ca70-3244-450c-adce-b6fb5982743e

Public Version Date

June 05, 2020

Public Version Number

3

DI Record Publish Date

June 23, 2018

Package DI Number

10884527018819

Quantity per Package

50

Contains DI Package

20884527018816

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE