DEVICE: Quantum (05060434422040)
Device Identifier (DI) Information
Quantum
QPF2
In Commercial Distribution
51-000025-01
SPECTRUM MEDICAL LIMITED
QPF2
In Commercial Distribution
51-000025-01
SPECTRUM MEDICAL LIMITED
Quantum Pump Frame 2 - Cheltenham
Device Characteristics
| Labeling does not contain MRI Safety Information | |
| No | |
| No | |
| No | |
| Yes | |
| No | |
| No | |
| No | |
| No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
| GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
|---|---|---|---|---|
| 36347 | Cardiopulmonary bypass system roller pump |
A mains electricity (AC-powered) device that is a module of a cardiopulmonary bypass system and is used to circulate the blood flow outside of the body for gas exchange and reinfusion via a roller type mechanism. It may be designed with a single or a dual rotor head that presses the blood through the extracorporeal tubing set that is connected to the oxygenator and other parts of the heart-lung bypass system. This pump can also be used to deliver cardioplegia solution at a controlled volume to the patient.
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Active | false |
FDA Product Code
[?]| Product Code | Product Code Name |
|---|---|
| DTQ | Console, Heart-Lung Machine, Cardiopulmonary Bypass |
FDA Premarket Submission
| FDA Premarket Submission Number [?] | Supplement Number [?] |
|---|---|
| K173834 | 000 |
Sterilization
Storage and Handling
[?]| Storage and Handling |
|---|
| Handling Environment Atmospheric Pressure: between 76 and 106 KiloPascal |
| Handling Environment Humidity: between 0 and 90 Percent (%) Relative Humidity |
| Handling Environment Temperature: between 0 and 6 Degrees Celsius |
Clinically Relevant Size
[?]| Size Type Text |
|---|
| No Device Sizes |
Device Record Status
69282a85-ad5a-4a1c-a41d-cda9baa06610
April 13, 2021
1
April 05, 2021
April 13, 2021
1
April 05, 2021
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]| Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
|---|---|---|---|---|---|
| No Package DIs found | |||||
Secondary DI
[?]| Issuing Agency [?] | Secondary DI Number |
|---|---|
| No Secondary DIs found | |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
+441242650120
eusales@spectrummedical.com 800 265 2331
ussales@spectrummedical.com
eusales@spectrummedical.com 800 265 2331
ussales@spectrummedical.com