Catalog Number

-

Brand Name

PremierPro

Version/Model Number

3403

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

-

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

K101952,K101952

Product Code

ITX

Product Code Name

Transducer, Ultrasonic, Diagnostic

Public Device Record Key

40a447ef-e86a-463b-b9dd-7e06d3df6b61

Public Version Date

June 10, 2022

Public Version Number

4

DI Record Publish Date

June 01, 2016

Package DI Number

10818566012828

Quantity per Package

12

Contains DI Package

00818566012821

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case