Catalog Number

SSIP90068

Brand Name

SE12-3 Gen I®

Version/Model Number

SSIP90068

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K142100

Product Code

ITX

Product Code Name

Transducer, ultrasonic, diagnostic

Public Device Record Key

d1592e91-e8c3-41d3-b768-0e562f5a3691

Public Version Date

July 06, 2018

Public Version Number

4

DI Record Publish Date

October 17, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-