Catalog Number

BP-10F-DP-350/A

Brand Name

Brighton™

Version/Model Number

00884450088685

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"

-

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

KNS

Product Code Name

Unit, electrosurgical, endoscopic (with or without accessories)

Public Device Record Key

cdefe37d-14e8-43de-9fde-cf2f6c5e64e9

Public Version Date

March 22, 2019

Public Version Number

3

DI Record Publish Date

September 24, 2016

Package DI Number

10884450088682

Quantity per Package

5

Contains DI Package

00884450088685

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-