Catalog Number

194382

Brand Name

Tristar Manifold Kit # 1

Version/Model Number

194382

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

OEZ

Product Code Name

Cardiovascular Procedure Kit

Public Device Record Key

9b8a70c4-86e3-41bd-aa20-0e97fc6376f1

Public Version Date

January 23, 2019

Public Version Number

3

DI Record Publish Date

September 23, 2016

Package DI Number

20886333207842

Quantity per Package

20

Contains DI Package

00886333207848

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box