Catalog Number

-

Brand Name

T-3 Triple Lumen CT

Version/Model Number

MC013502

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

NIE

Product Code Name

CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED

Public Device Record Key

b6b9d0b0-d4e7-4eab-ad4a-82af9886c416

Public Version Date

July 15, 2022

Public Version Number

6

DI Record Publish Date

October 23, 2015

Package DI Number

50884908092757

Quantity per Package

5

Contains DI Package

00884908092752

Package Discontinue Date

January 29, 2021

Package Status

Not in Commercial Distribution

Package Type

box