CardioQuip Thermoelectric Cooling (TEC) Lid Module

GUDID 00860000846134

The Thermo-Electric Cooling (TEC) lid Module is used in conjunction with the CardioQuip Modular Cooler-Heater (MCH) to provide cooling to slow the melting of ice in the tank. The MCH is indicated to supply temperature-controlled water to heat exchange devices (e.g.; CPB Heat Exchangers, Cardioplegia Heat Exchangers and thermal regulating system blankets) to help control a patient's temperature during cardiopulmonary bypass procedures lasting not longer than six hours.

CARDIOQUIP, LLC

Cardiopulmonary bypass system heating/cooling unit Cardiopulmonary bypass system heating/cooling unit Cardiopulmonary bypass system heating/cooling unit Cardiopulmonary bypass system heating/cooling unit Cardiopulmonary bypass system heating/cooling unit Cardiopulmonary bypass system heating/cooling unit Cardiopulmonary bypass system heating/cooling unit Cardiopulmonary bypass system heating/cooling unit Cardiopulmonary bypass system heating/cooling unit Cardiopulmonary bypass system heating/cooling unit Cardiopulmonary bypass system heating/cooling unit Cardiopulmonary bypass system heating/cooling unit Cardiopulmonary bypass system heating/cooling unit Cardiopulmonary bypass system heating/cooling unit
Primary Device ID00860000846134
NIH Device Record Keydc823d46-1588-4af4-a797-7dc750a03e1a
Commercial Distribution StatusIn Commercial Distribution
Brand NameCardioQuip Thermoelectric Cooling (TEC) Lid Module
Version Model NumberMCH-11TEC
Company DUNS144183733
Company NameCARDIOQUIP, LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100860000846134 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DWCController, Temperature, Cardiopulmonary Bypass

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-12-16
Device Publish Date2020-12-08

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