Catalog Number

-

Brand Name

DeRoyal

Version/Model Number

89-2995

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

OHD

Product Code Name

Gynecological laparoscopic kit

Public Device Record Key

881af56c-1221-4099-9490-11372e7c7f3c

Public Version Date

October 22, 2018

Public Version Number

3

DI Record Publish Date

September 12, 2016

Package DI Number

50749756308804

Quantity per Package

6

Contains DI Package

00749756308809

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case