QUICKIE PRIME - 24" W/CLAMP - A sterile, semi-rigid tube used in open heart - NOVOSCI CORP.

Duns Number:938289980

Device Description: A sterile, semi-rigid tube used in open heart surgery to facilitate the transfer of primin A sterile, semi-rigid tube used in open heart surgery to facilitate the transfer of priming fluids during the priming of the extracorporeal circuit of a cardiopulmonary bypass system. It is a noninvasive product in the form of a tube or tubing used to channel the fluids (i.e., primer/blood) to facilitate priming of the extracorporeal circuit and connection of the cardiopulmonary bypass system (heart/lung machine) to the patient. It is typically a moulded plastic tube with hard plastic spike at the distal end that connects to the bag or container of primer solution, a connector at the proximal end, and a central pinch clamp. This is a single-use device.

Want to know more about this Product? Request more information now!


More Product Details

Catalog Number

301124-000

Brand Name

QUICKIE PRIME - 24" W/CLAMP

Version/Model Number

301124-000

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

Product Characteristics

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

K801402,K801402

Product Code Details

Product Code

DTL

Product Code Name

Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass

Device Record Status

Public Device Record Key

2a6dacfd-bdaf-4fd5-8920-e105092a4556

Public Version Date

March 10, 2022

Public Version Number

5

DI Record Publish Date

September 26, 2016

Additional Identifiers

Package DI Number

B0663011240006

Quantity per Package

25

Contains DI Package

B0663011240000

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE

"NOVOSCI CORP." Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 50