Catalog Number

31142717

Brand Name

Devon

Version/Model Number

31142717

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

d1226e0c-1de4-4c99-b1ad-71d0cc2b1a0b

Public Version Date

October 21, 2020

Public Version Number

3

DI Record Publish Date

June 30, 2018

Package DI Number

10884527015849

Quantity per Package

240

Contains DI Package

10884521512658

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE