Catalog Number

31142352

Brand Name

Devon

Version/Model Number

31142352

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

GAB

Product Code Name

NEEDLE, SUTURING, DISPOSABLE

Public Device Record Key

4f3fd88e-56a3-4bc4-a3e3-6638ed325947

Public Version Date

January 08, 2021

Public Version Number

3

DI Record Publish Date

June 23, 2018

Package DI Number

20884527016393

Quantity per Package

64

Contains DI Package

30884527016390

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE