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ThermoGenesis Announces Receipt of CE Mark for MarrowXpress(TM)
Date:6/19/2008

Approval Allows Company to Begin Commercial Sales of Device in Europe

RANCHO CORDOA, Calif., June 19 /PRNewswire-FirstCall/ -- ThermoGenesis Corp. (Nasdaq: KOOL), a leading supplier of innovative products and services that process and store adult stem cells, today announced TUV has issued an EC Certificate to ThermoGenesis Corp. for the MarrowXpress (MXP(TM)) System, which allows the Company to affix the CE Mark and commence selling the product in the European Community. The MXP device is used to process bone marrow in a laboratory setting.

The MXP is a derivative of the Company's approved AutoXpress(TM) (AXP(TM)) Platform that is used to volume reduce and collect stem cells from umbilical cord blood. Earlier this month, ThermoGenesis announced it had submitted a 510(k) pre-market notification application to the FDA seeking regulatory clearance in the U.S.

"We have had very encouraging feedback from a number of European centers at which bone marrow clinical trials are either underway or planned. With this approval, we can now ramp up those discussions and initiate a formal launch for the MXP in Europe," noted Dr. William Osgood, Chief Executive Officer of ThermoGenesis.

"There are a number of clinical trials already underway, as well as the practice of medicine, evaluating the use of adult stems cells to treat indications such as critical limb ischemia, coronary artery disease and orthopedic conditions. We believe the collection of stem cells from bone marrow could ultimately represent a multi-billion dollar market opportunity for the Company," he added.

About ThermoGenesis Corp.

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SOURCE ThermoGenesis Corp.
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