Catalog Number

31372223

Brand Name

Devon

Version/Model Number

31372223

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

FSM

Product Code Name

TRAY, SURGICAL, INSTRUMENT

Public Device Record Key

ce2ae4d8-18c3-4772-be32-462b12f8d9e8

Public Version Date

February 15, 2019

Public Version Number

2

DI Record Publish Date

June 23, 2018

Package DI Number

10884527020164

Quantity per Package

20

Contains DI Package

20884527020161

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE