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Normothermic Machine Perfusion System For The Preservation Of Standard Criteria Donor Lungs Prior To Transplantation

Page Type
Product Code
Definition
To preserve donor lungs prior to transplantation
Physical State
The device may consists of a portable enclosure with electronics and hardcore that control the ventilation and perfusion of the donor organ, disposable components that complete the ventilation and perfusion circuits, and a preservation solution used to perfuse the organ.
Technical Method
The device perfuses and ventilates the donor lungs prior to transplantation
Target Area
Donor lungs
Review Panel
Gastroenterology and Urology
Submission Type
PMA
Device Classification
Class 3
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

The FDA has not linked product code QBA to any particular section of the CFR (Code of Federal Regulations). There are multiple reasons why this might be the case:

  • The product code was created for a class III submission that does not follow the normal PMN or PMA path - e.g., for a device that falls under HDE (Humanitarian Device Exemption) or EUA (Emergency Use Authorization).
  • The FDA has generated the product code for an existing Class III device, as a result of a PMA supplement that modifies the device in a way that it can't fit under the existing product code originally assigned
  • The product code was created for internal use at the FDA, and not for classification or regulatory-related purposes.

Normothermic Machine Perfusion System For The Preservation Of Standard Criteria Donor Lungs Prior To Transplantation

Page Type
Product Code
Definition
To preserve donor lungs prior to transplantation
Physical State
The device may consists of a portable enclosure with electronics and hardcore that control the ventilation and perfusion of the donor organ, disposable components that complete the ventilation and perfusion circuits, and a preservation solution used to perfuse the organ.
Technical Method
The device perfuses and ventilates the donor lungs prior to transplantation
Target Area
Donor lungs
Review Panel
Gastroenterology and Urology
Submission Type
PMA
Device Classification
Class 3
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

The FDA has not linked product code QBA to any particular section of the CFR (Code of Federal Regulations). There are multiple reasons why this might be the case:

  • The product code was created for a class III submission that does not follow the normal PMN or PMA path - e.g., for a device that falls under HDE (Humanitarian Device Exemption) or EUA (Emergency Use Authorization).
  • The FDA has generated the product code for an existing Class III device, as a result of a PMA supplement that modifies the device in a way that it can't fit under the existing product code originally assigned
  • The product code was created for internal use at the FDA, and not for classification or regulatory-related purposes.