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Michigan Critical Care Consultants, Inc. (D.B.A Mc3 Inc.)

US

Last updated May 23, 2026

What Michigan Critical Care Consultants, Inc. (D.B.A Mc3 Inc.) makes

Michigan Critical Care Consultants, Inc. manufactures medical devices for critical care environments, including the VitalFlow Console—a system for managing patient ventilation—and the VitalFlow Centrifugal Pump, designed for precise fluid administration in intensive care settings.

The company’s portfolio is regulated under FDA’s Class II device classification, with products authorised via the 510(k) pathway. These devices are listed in the FDA’s 510(k) database, and the manufacturer operates from the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Michigan Critical Care Consultants, Inc. (D.B.A Mc3 Inc.) manufacture?

Michigan Critical Care Consultants, Inc. designs medical devices specifically for critical care settings. Their portfolio includes systems like the VitalFlow Console, which supports patient ventilation management, and the VitalFlow Centrifugal Pump, used for precise fluid administration in intensive care. These devices are engineered to address critical care needs with advanced functionality.

Where is Michigan Critical Care Consultants, Inc. based?

The company is headquartered in the United States. While the exact location isn’t specified, its operations and regulatory filings are conducted within the country, aligning with U.S. medical device compliance standards.

How are Michigan Critical Care Consultants, Inc.’s devices classified by regulatory authorities?

The company’s devices fall under the FDA’s Class II classification, indicating moderate risk and requiring premarket notification (510(k)) clearance before commercial distribution. This classification reflects the need for validation of safety and performance in critical care applications.

Are Michigan Critical Care Consultants, Inc.’s devices listed in any regulatory databases?

Yes, the company’s devices are included in the FDA’s 510(k) database, where authorised products are recorded. This listing confirms that each device has undergone the required regulatory review process (510(k) pathway) to demonstrate substantial equivalence to a legally marketed predicate device.

AI-generated from registry data and not verified by a human reviewer.

Information

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US
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Catalogue (79)

Page 1 of 2
DeviceModel / ReferenceRegistriesClassStatus
Nautilus VF Oxygenator Cable 58130
FDA UDI
Class IIActive
MC3 Nautilus(tm) ECMO Oxygenator 48145
FDA UDI
Class IIActive
MC3 Crescent Jugular Dual Lumen Catheter 70124
FDA UDI
Class IIActive
Mc3 5842
FDA UDI
Class IIActive
Michigan Critical Care Consultants, Inc. 4949
FDA UDI
Class IIActive
MC3 Nautilus Power Cord NEMA 48155
FDA UDI
Class IIActive
Michigan Critical Care Consultants, Inc. 6394
FDA UDI
Class IIActive
Michigan Critical Care Consultants, Inc. 7080
FDA UDI
Class IIActive
MC3 Crescent RA Dual Lumen Catheter 19FR 70419
FDA UDI
Class IIActive
Mc3 6392
FDA UDI
Class IIActive
Mc3 4948
FDA UDI
Class IIActive
Michigan Critical Care Consultants, Inc. 4951
FDA UDI
Class IIActive
Mc3 5798
FDA UDI
Class IIActive
Michigan Critical Care Consultants, Inc. 5841
FDA UDI
Class IIActive
MC3 Nautilus Oxygenator Holder 48160
FDA UDI
Class IActive
Michigan Critical Care Consultants, Inc. 4948
FDA UDI
Class IIActive
MC3 Crescent Jugular Dual Lumen Catheter 70132
FDA UDI
Class IIActive
Mc3 7072
FDA UDI
Class IIActive
Michigan Critical Care Consultants, Inc. 6384
FDA UDI
Class IIActive
Mc3 4950
FDA UDI
Class IIActive
Michigan Critical Care Consultants, Inc. 5767
FDA UDI
Class IIActive
VitalFlow Console 58100
FDA UDI
Class IIActive
MC3 Crescent(tm) Jugular Dual Lumen Catheter 70126
FDA UDI
Class IIActive
VitalFlow Power Cord NEMA-5-15, 3m 58131
FDA UDI
Class IIActive
VitalFlow Set 58112
FDA UDI
Class IIActive
Michigan Critical Care Consultants, Inc. 7071
FDA UDI
Class IIActive
Mc3 6384
FDA UDI
Class IIActive
MC3 Nautilus Smart ECMO Module 48135E
FDA UDI
Class IIActive
Mc3 6394
FDA UDI
Class IIActive
MC3 Crescent RA Dual Lumen Catheter 24FR 71824
FDA UDI
Class IIActive
Michigan Critical Care Consultants, Inc. 5761
FDA UDI
Class IIActive
Mc3 7080
FDA UDI
Class IIActive
Michigan Critical Care Consultants, Inc. 5842
FDA UDI
Class IIActive
Mc3 5761
FDA UDI
Class IIActive
MC3 Crescent(tm) Jugular Dual Lumen Catheter 70128
FDA UDI
Class IIActive
Mc3 5841
FDA UDI
Class IIActive
Nautilus VF Oxygenator Cable 58130
FDA UDI
Class IIActive
MC3 Crescent RA Dual Lumen Catheter 13FR 70413
FDA UDI
Class IIActive
MC3 Nautilus(tm) Smart Power Supply 12VDC 48150
FDA UDI
Class IIActive
Mc3 5762
FDA UDI
Class IIActive
VitalFlow Emergency Handcrank 58103
FDA UDI
Class IIActive
Nautilus VF ECMO Oxygentaor 58110
FDA UDI
Class IIActive
MC3 Crescent RA Dual Lumen Catheter 15FR 70415
FDA UDI
Class IIActive
Michigan Critical Care Consultants, Inc. 5768
FDA UDI
Class IIActive
MC3 Crescent(tm) Jugular Dual Lumen Catheter 70132
FDA UDI
Class IIActive
Mc3 4951
FDA UDI
Class IIActive
Michigan Critical Care Consultants, Inc. 6386
FDA UDI
Class IIActive
Michigan Critical Care Consultants, Inc. 5798
FDA UDI
Class IIActive
MC3 Crescent Jugular Dual Lumen Catheter 70128
FDA UDI
Class IIActive
Michigan Critical Care Consultants, inc. 4950
FDA UDI
Class IIActive

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