Catalog Number

-

Brand Name

DeRoyal

Version/Model Number

35-300692

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

DQO

Product Code Name

CATHETER, INTRAVASCULAR, DIAGNOSTIC

Public Device Record Key

e5c30bde-927a-4e99-aab0-ba817cdfc7b4

Public Version Date

August 11, 2021

Public Version Number

3

DI Record Publish Date

September 12, 2016

Package DI Number

50749756230136

Quantity per Package

80

Contains DI Package

00749756230131

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case