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SPECTRUM MEDICAL LIMITED

US

Last updated May 24, 2026

What SPECTRUM MEDICAL LIMITED makes

Spectrum Medical Limited manufactures components and systems for cardiopulmonary bypass and extracorporeal membrane oxygenation (ECMO) procedures. Their portfolio includes air bubble and fluid level detectors, blood gas/pH monitors, single-use heat exchangers, membrane oxygenators, gas control units, roller pumps, drainage cannulae, and centrifugal pumps. The Quantum series is central to their offerings, with variations tailored for specific clinical applications.

The company’s devices are classified under FDA regulations as Class I and Class II, with relevant products listed in the FDA’s Unique Device Identifier (UDI) database. Spectrum Medical Limited is based in the United States, adhering to applicable regulatory standards for medical devices in that jurisdiction.

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 Spectrum Medical Limited manufacture?

Spectrum Medical Limited specializes in devices used for cardiopulmonary bypass and extracorporeal membrane oxygenation (ECMO) procedures. Their portfolio includes critical components like air bubble and fluid level detectors, blood gas/pH monitors, single-use heat exchangers, membrane oxygenators, gas control units, roller pumps, drainage cannulae, and centrifugal pumps. These devices support life-saving interventions by ensuring precise control of blood flow, oxygenation, and temperature during surgery or critical care.

Where is Spectrum Medical Limited based, and does that affect the regulatory standards they follow?

Spectrum Medical Limited is based in the United States. As a U.S.-based manufacturer, their devices must comply with FDA regulations, including classification under Class I or Class II. This classification determines the level of scrutiny and regulatory requirements for each device type, ensuring safety and performance standards are met before market entry.

Which regulatory registries or databases list Spectrum Medical Limited’s devices?

Spectrum Medical Limited’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system provides a standardized way to identify medical devices, ensuring transparency and traceability for healthcare providers, regulators, and patients. This listing helps streamline tracking and compliance with U.S. regulatory requirements.

How are Spectrum Medical Limited’s devices classified under FDA regulations?

Spectrum Medical Limited’s devices are classified under the FDA’s regulatory framework as either Class I or Class II. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve a higher risk and require additional performance standards or special controls. The classification ensures appropriate oversight based on the device’s intended use and potential risk to patients.

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

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
+441242650120
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
516398679

Catalogue (226)

Page 1 of 5
DeviceModel / ReferenceRegistriesClassStatus
Quantum QFS3-ST-075
FDA UDI
Class IIActive
Quantum QCD37
FDA UDI
Class IIActive
Quantum QFS3-RA-150
FDA UDI
Class IIActive
Quantum QWS15S
FDA UDI
Class IIActive
Quantum QPR2
FDA UDI
Class IIActive
Quantum PureFlow Standard Heat Exchanger High Flow 3/8 HX55W-S0
FDA UDI
Class IIActive
Quantum QFS4-RA-150
FDA UDI
Class IIActive
Quantum QPR3
FDA UDI
Class IIActive
Quantum QPF3
FDA UDI
Class IIActive
Quantum SuperPAC Cardioplegia Set 1/4 CGSP2-B0
FDA UDI
Class IIUnknown
Quantum QPR4
FDA UDI
Class IIActive
Quantum QPF2
EUDAMEDFDA UDI
Class IIActive
Quantum QPF4
EUDAMEDFDA UDI
Class IIActive
Quantum QPR1
FDA UDI
Class IIActive
Quantum 52-000096-00
EUDAMEDFDA UDI
Class IIActive
Quantum QFS3-RA-060
FDA UDI
Class IIActive
Quantum QFS1-ST-120
FDA UDI
Class IIActive
Quantum Perfusion Blood Oxygenator with Integrated AF VT200-C2 VT200-C2
FDA UDI
Class IIActive
Quantum QFS4-ST-300
FDA UDI
Class IIActive
Quantum QFS2-ST-075
FDA UDI
Class IIActive
Quantum SuperPAC Tubing Set - SP02C-DA SP02C-DA
FDA UDI
Class IIUnknown
System M ® Gas Management System
FDA UDI
Class IIUnknown
System M ® M4
FDA UDI
Class IIUnknown
Quantum QFS7-ST-075
FDA UDI
Class IIActive
Quantum QLV1
FDA UDI
Class IIActive
Quantum QFS3-ST-120
FDA UDI
Class IIActive
System M ® Gas Module
FDA UDI
Class IIUnknown
System M ® Gas Management System
FDA UDI
Class IIUnknown
Quantum Perfusion Dual Lumen Cannula 27 DL27F-V0
FDA UDI
Class IIActive
Quantum QDE
FDA UDI
Class IIActive
Quantum ® QPF2
FDA UDI
Class IIActive
Quantum SuperPAC CPB – 3/8 Venous with AV Bridge SPC200A-D4
FDA UDI
N/AActive
KIT Quantum SuperPAC Tubing Set - 160 SPC-160
FDA UDI
Class IIUnknown
Quantum QFS5-ST-120
FDA UDI
Class IIActive
Quantum QSOR
FDA UDI
Class IIActive
System M ® VIPER DM
FDA UDI
Class IUnknown
Quantum Perfusion Centrifugal Blood Pump CP20NG with Integrated Sensors CP20V-NG
FDA UDI
Class IIActive
Quantum QFS2-RA-075
FDA UDI
Class IIActive
Quantum ® QPF1
FDA UDI
Class IIActive
Quantum Perfusion Blood Oxygenator with Integrated AF VT75-C2U VT75-C2U
FDA UDI
Class IIActive
Quantum Perfusion Blood Oxygenator with Integrated AF and Sensor VT75-C1U VT75-C1U
FDA UDI
Class IIActive
Quantum ® System M ® HBS4-200
FDA UDI
Class IIActive
Quantum ® System M ® Flow & Emboli Sensor
FDA UDI
Class IIActive
Quantum HBS2-050
FDA UDI
Class IIActive
Quantum QFS6-ST-200
FDA UDI
Class IIActive
Quantum QPR5
FDA UDI
Class IIActive
Quantum PureFlow Standard Heat Exchanger Low Flow 3/16 HX11W-S0
FDA UDI
Class IIActive
Quantum QVM
FDA UDI
Class IIActive
Quantum 52-000044-00
EUDAMEDFDA UDI
Class IIActive
Quantum LSC_HRF
EUDAMEDFDA UDI
Class IActive

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Spectrum Medical Ltd GLOUCESTER Gloucestershire · GB FEI 3006073153