← Back to catalogue

CardioQuip Modular Cooler-Heater (MCH)

FDA UDI

Class II (US FDA UDI)

by CardioQuip

Identity

Trade Name
CardioQuip Modular Cooler-Heater (MCH) FDA UDI
Generic Name
Cardiopulmonary bypass system heating/cooling unit FDA UDI
Device Name
The CardioQuip Modular Cooler-Heater (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. FDA UDI
Model / Reference
MCH-1000(i) FDA UDI
Description
The CardioQuip Modular Cooler-Heater (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. FDA UDI

Identifiers

Primary DI / UDI-DI
00860000846103 FDA UDI
510(k) Number
K102147 FDA UDI
FDA Product Code
DWC FDA UDI
GMDN Term
Cardiopulmonary bypass system heating/cooling unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4250 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cardiopulmonary bypass system heating/cooling unit

CardioQuip Modular Cooler-Heater (MCH) by CardioQuip — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiopulmonary bypass system heating/cooling unit.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
CardioQuip

Sources (1)

  • FDA UDI 090efd33-0527-4480-a5c3-5fdb238e9369 34 fields · synced Jun 8, 2026