Catalog Number

5450-800-302

Brand Name

NA

Version/Model Number

5450800302

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

LFL

Product Code Name

Instrument, ultrasonic surgical

Public Device Record Key

16f111cb-b54b-42b5-b0fd-717da5ee60c7

Public Version Date

August 06, 2019

Public Version Number

3

DI Record Publish Date

September 23, 2016

Package DI Number

37613252026625

Quantity per Package

5

Contains DI Package

07613252026624

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

pack