Catalog Number

31460200

Brand Name

Devon

Version/Model Number

31460200

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

0dc16406-8dc6-4a86-a965-e0b8735faf7d

Public Version Date

November 19, 2020

Public Version Number

3

DI Record Publish Date

June 23, 2018

Package DI Number

10884527014460

Quantity per Package

6

Contains DI Package

20884527014467

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE