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CentriMag
TM
Circulatory Support System Operation Manual (US)
Page 8 of 126
© 2019 Abbott – Document No PL-0047, Rev 11 (December 2019)
Indications for Use Chart
Product Name and
Market Application
Number
Refer to Label Part
No.
Required US
Caution
Statement(s)
Indications for Use
Pump
K090051
Blood Pump IFU
restricts this device
to sale, distribution
and use by or on the
order of a physician.
Pump is indicated
for use only with the
2
nd
Generation
CentriMag Primary
Console to pump
blood through the
extracorporeal
bypass circuit for
extracorporeal
circulatory support
for periods ap-
propriate to
cardiopulmonary
bypass (CPB) for up
to six hours. It is
also indicated for
use in
extracorporeal
support systems (for
periods up to six
hours) not requiring
complete CPB (e.g.
valvuloplasty,
circulatory support
during mitral valve
reoperation, surgery
of the vena cava or
aorta, liver
transplants etc.)
This device is not
designed, sold, or
intended for use
except as indicated.
CentriMag Drainage
(Venous) Cannula
Kit
K110983
K152190
PL-0220, CentriMag
Drainage (Venous)
Cannula Kit IFU
Federal (U.S.A.) law
restricts this device
to sale, distribution
and use by or on the
order of a physician.
The CentriMag
Drainage (Venous)
Cannula is indicated
for use with an
extracorporeal
bypass circuit for
extracorporeal
circulatory support
for periods up to six
hours.
CentriMag Return
(Arterial) Cannula
Kit
K110980
PL-0221, CentriMag
Return (Arterial)
Cannula Kit IFU
Federal (U.S.A.) law
restricts this device
to sale, distribution
and use by or on the
order of a physician.
The CentriMag
Return (Arterial)
Cannula is indicated
for use as an arterial
return cannula with
an extracorporeal