Designed by University of California, Los Angeles in 2001, MERCI was the first device approved in the U.S. to remove blood clots in patients who had acute brain ischemia.
[2] In this carefully selected group it achieved 48% vessel re-canalization[2] and lower mortality rates than the use of r-tPA in revascularized patients.
The retriever consists of a long thin wire with a helical coil formed at the distal end.
[3] The MERCI Retriever obtained U.S. FDA clearance in August 2004 for re-canalization of cerebral arteries in acute stroke.
[2] Concentric Medical undertook a preliminary study of the MERCI retriever to assess its effectiveness.