Catalog Number

-

Brand Name

DeRoyal

Version/Model Number

89-9265

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

OEQ

Product Code Name

Angiography/angioplasty kit

Public Device Record Key

1a15fdc5-4b5a-4738-a1f2-e408040f40aa

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

November 05, 2017

Package DI Number

50749756941797

Quantity per Package

6

Contains DI Package

00749756941792

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case