Catalog Number

-

Brand Name

Busse Hospital Disposables

Version/Model Number

1592

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FSM

Product Code Name

Tray, Surgical, Instrument

Public Device Record Key

69152686-a45c-43ff-b93d-622f955bccf1

Public Version Date

June 17, 2022

Public Version Number

2

DI Record Publish Date

September 28, 2021

Package DI Number

10849233006154

Quantity per Package

10

Contains DI Package

00849233006157

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-