Catalog Number

-

Brand Name

Transonic

Version/Model Number

ADT1001-10

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

November 01, 2021

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

DYG

Product Code Name

Catheter, Flow Directed

Public Device Record Key

1b81fc45-c960-4cab-aa61-258582ab5371

Public Version Date

November 05, 2021

Public Version Number

3

DI Record Publish Date

April 28, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-