Catalog Number

89-10729

Brand Name

DeRoyal

Version/Model Number

89-10729

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

KDD

Product Code Name

Kit, surgical instrument, disposable

Public Device Record Key

2a66201e-49ac-4086-94ca-bc3c0d0c3e11

Public Version Date

June 17, 2022

Public Version Number

2

DI Record Publish Date

September 21, 2021

Package DI Number

50749756376087

Quantity per Package

6

Contains DI Package

00749756376082

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case