Catalog Number

-

Brand Name

DeRoyal

Version/Model Number

50-501

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"

Yes

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

OVN

Product Code Name

Suture kit

Public Device Record Key

83568eae-0634-487d-985d-76c3006083e9

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

April 18, 2017

Package DI Number

50749756276660

Quantity per Package

20

Contains DI Package

00749756276665

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case