Catalog Number

-

Brand Name

Buzz 2.0

Version/Model Number

15800A

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

-

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

-

Product Code

LMD

Product Code Name

System, Digital Image Communications, Radiological

Public Device Record Key

ba14dc2e-a5d4-493e-be21-50f5f7d06f0f

Public Version Date

January 05, 2021

Public Version Number

1

DI Record Publish Date

December 28, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-