Catalog Number

040151

Brand Name

Carbon Bright®

Version/Model Number

040151

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K132064,K132064

Product Code

IYE

Product Code Name

Accelerator, Linear, Medical

Public Device Record Key

0b8e68ba-a2d9-4e2c-b2b4-e6b5c79427ec

Public Version Date

June 10, 2022

Public Version Number

2

DI Record Publish Date

January 08, 2020

Package DI Number

10850002461043

Quantity per Package

10

Contains DI Package

00850002461046

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton