Capturing Clot Without The Wait CHAPLA
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INDICATIONS FOR USE: The ERIC® Retrieval Device is intended for use in the revascularization of acute ischemic stroke caused by the intracranial occlusive vessels of patients who are not eligible for intravenous tissue plasminogen activator, IV tPA, or who fail IV tPA therapy.
MICROVENTION, ERIC, SOFIA and Headway are registered trademarks of MicroVention, Inc. Refer to Instructions for Use, contraindications and warnings for additional information. © 2016 MicroVention, Inc. MM507(i) EMEA 8/16
Capturing Clot
100
90
80
70
60
50
40
30
20
10
0
ERIC®
TICI 2a11.1%
TICI 2b30.6%
TICI 352.8%
TICI 2a-3 Revascularization
70
60
50
40
30
20
10
0
ERIC®
mRS 0-233.3%
mRS 325.0%
mRS 0-3 @ 90 Days
Initial clinical experience with the ERIC® device is in line with other peer reviewed, published data on mechanical thrombectomy.
ERIC 3x20
ERIC 4x24
ERIC 4x30
ERIC 6x35
ERIC 6x44
3mm
4mm
4mm
6mm
6mm
203cm
203cm
203cm
203cm
203cm
Distal M2/M3
M1/M2
M1/M2
Proximal M1/ICA
Proximal M1/ICA
PRODUCT PRODUCTCODE
DIAMETER(A)
WORKINGLENGTH
(B)
NUMBEROF
SPHERES
MINIMUMCATHETER ID
(D)
RECOMMENDEDVESSEL
LOCATION
DISTAL TIPLENGTH
(C)
PUSHERLENGTH
(E)
5.0mm
5.0mm
5.0mm
5.0mm
5.0mm
4
4
5
4
5
20mm
24mm
30mm
35mm
44mm
0.017”
0.017”
0.017”
0.017”
0.017”
The MicroVention Stroke System
ER173020
ER174024
ER174030
ER176035
ER176044
A = Diameter
B = Working Length E = Pusher Length
C =Distal TipLength
D =MinimumCatheter
ID
Without The Wait
ERIC is compatible with:
MicroVention, Inc., Worldwide Headquarters, 1311 Valencia Avenue, Tustin, CA 92780 USA Phone: 714.247.8000 Customer Service: 800.990.8368
microvention.com
CHAPLA
INDICATIONS FOR USE: The ERIC® Retrieval Device is intended for use in the revascularization of acute ischemic stroke caused by the intracranial occlusive vessels of patients who are not eligible for intravenous tissue plasminogen activator, IV tPA, or who fail IV tPA therapy.
MICROVENTION, ERIC, SOFIA and Headway are registered trademarks of MicroVention, Inc. Refer to Instructions for Use, contraindications and warnings for additional information. © 2016 MicroVention, Inc. MM507(i) EMEA 8/16
microvention.com
MicroVention, Inc. Worldwide Headquarters1311 Valencia AvenueTustin, CA 92780 USA PH +1.714.247.8000 PH 1.800.990.8368
MicroVention UK LimitedSuite 3, The Barracks Building10 Cliffords Fort, North ShieldsTyne and Wear, NE30 1JEUnited KingdomPH +44 (0) 191 258 6777F +44 (0) 191 258 5999
MicroVention Europe, S.A.R.L.30 bis, rue du Vieil Abreuvoir78100 Saint-Germain-en-LayeFrancePH +33 (1) 39 21 77 46F +33 (1) 39 21 16 01
MicroVention Deutschland GmbHHildebrandtstr. 4 FD-40215 DüsseldorfGermanyPH +49 211 210 798-0F +49 211 210 798-29
Capturing Clot
100
90
80
70
60
50
40
30
20
10
0
ERIC®
TICI 2a11.1%
TICI 2b30.6%
TICI 352.8%
TICI 2a-3 Revascularization
70
60
50
40
30
20
10
0
ERIC®
mRS 0-233.3%
mRS 325.0%
mRS 0-3 @ 90 Days
Initial clinical experience with the ERIC® device is in line with other peer reviewed, published data on mechanical thrombectomy.
ERIC 3x20
ERIC 4x24
ERIC 4x30
ERIC 6x35
ERIC 6x44
3mm
4mm
4mm
6mm
6mm
203cm
203cm
203cm
203cm
203cm
Distal M2/M3
M1/M2
M1/M2
Proximal M1/ICA
Proximal M1/ICA
PRODUCT PRODUCTCODE
DIAMETER(A)
WORKINGLENGTH
(B)
NUMBEROF
SPHERES
MINIMUMCATHETER ID
(D)
RECOMMENDEDVESSEL
LOCATION
DISTAL TIPLENGTH
(C)
PUSHERLENGTH
(E)
5.0mm
5.0mm
5.0mm
5.0mm
5.0mm
4
4
5
4
5
20mm
24mm
30mm
35mm
44mm
0.017”
0.017”
0.017”
0.017”
0.017”
The MicroVention Stroke System
ER173020
ER174024
ER174030
ER176035
ER176044
A = Diameter
B = Working Length E = Pusher Length
C =Distal TipLength
D =MinimumCatheter
ID
Without The Wait
ERIC is compatible with:
EMEA
Adjustable Working Length
ERIC “plunging”action into SOFIA
SOFIA movingdistal toward ERIC and clot
Maintain aspirationuntil complete device removal
Why wait?
30
25
20
15
10
5
0
ERIC®
25.4%
TRADITIONALSTENTRIEVERS
INTRALUMENAL CLOT CAPTURE SURFACE
0.7%
Greater surface areain the axial directionmakes it easier to retrieve thrombus.
10
5
0
ERIC®
7.5%
TRADITIONALSTENTRIEVERS
LATERAL CLOT CAPTURE SURFACE
Greater surface area in the lateral direction increases clot integration time.
0.8%
The ERIC device works in conjunction with the SOFIA® Plus catheter to assist aspiration; acting as a conveyor belt to help retrieve clot into the powerful aspiration vacuum generated by the SOFIA Plus.
Traditional stentrievers “roll” the clot between the stentriever and the vessel wall.
Images Courtesy of Thomas Liebig, MD, University of Cologne, Cologne - GERMANY
Images Courtesy of Jens Fiehler, MD, University Medical Center Hamburg, Eppendorf - GERMANY
Images Courtesy of Caspar Brekenfield, MD, University of Hamburg, Hamburg - GERMANY
Pulling Vs. Rolling
Intralumenal clot capture surface eliminates wait time
INTRALUMENAL
INTRALUMENAL
LATERAL
LATERAL
Initial TICI Score: 0at 3:10 pm ERIC 6 x 44 Final TICI Score: 3 at 3:24 pm
After 2 Passes
Initial TICI Score: 0at 9:03 pm ERIC 4 x 30 Final TICI Score: 3 at 9:17 pm
After 1 Pass
The ability to select the number of working spheres allows for precise control
Initial TICI Score: 0NIHSS: 5
Partial Recanalisation withERIC 6 x 44 Placed in Occlusion Site
Final TICI Score: 3After 1 Pass
Adjustable Working Length
ERIC “plunging”action into SOFIA
SOFIA movingdistal toward ERIC and clot
Maintain aspirationuntil complete device removal
Why wait?
30
25
20
15
10
5
0
ERIC®
25.4%
TRADITIONALSTENTRIEVERS
INTRALUMENAL CLOT CAPTURE SURFACE
0.7%
Greater surface areain the axial directionmakes it easier to retrieve thrombus.
10
5
0
ERIC®
7.5%
TRADITIONALSTENTRIEVERS
LATERAL CLOT CAPTURE SURFACE
Greater surface area in the lateral direction increases clot integration time.
0.8%
The ERIC device works in conjunction with the SOFIA® Plus catheter to assist aspiration; acting as a conveyor belt to help retrieve clot into the powerful aspiration vacuum generated by the SOFIA Plus.
Traditional stentrievers “roll” the clot between the stentriever and the vessel wall.
Images Courtesy of Thomas Liebig, MD, University of Cologne, Cologne - GERMANY
Images Courtesy of Jens Fiehler, MD, University Medical Center Hamburg, Eppendorf - GERMANY
Images Courtesy of Caspar Brekenfield, MD, University of Hamburg, Hamburg - GERMANY
Pulling Vs. Rolling
Intralumenal clot capture surface eliminates wait time
INTRALUMENAL
INTRALUMENAL
LATERAL
LATERAL
Initial TICI Score: 0at 3:10 pm ERIC 6 x 44 Final TICI Score: 3 at 3:24 pm
After 2 Passes
Initial TICI Score: 0at 9:03 pm ERIC 4 x 30 Final TICI Score: 3 at 9:17 pm
After 1 Pass
The ability to select the number of working spheres allows for precise control
Initial TICI Score: 0NIHSS: 5
Partial Recanalisation withERIC 6 x 44 Placed in Occlusion Site
Final TICI Score: 3After 1 Pass
Adjustable Working Length
ERIC “plunging”action into SOFIA
SOFIA movingdistal toward ERIC and clot
Maintain aspirationuntil complete device removal
Why wait?
30
25
20
15
10
5
0
ERIC®
25.4%
TRADITIONALSTENTRIEVERS
INTRALUMENAL CLOT CAPTURE SURFACE
0.7%
Greater surface areain the axial directionmakes it easier to retrieve thrombus.
10
5
0
ERIC®
7.5%
TRADITIONALSTENTRIEVERS
LATERAL CLOT CAPTURE SURFACE
Greater surface area in the lateral direction increases clot integration time.
0.8%
The ERIC device works in conjunction with the SOFIA® Plus catheter to assist aspiration; acting as a conveyor belt to help retrieve clot into the powerful aspiration vacuum generated by the SOFIA Plus.
Traditional stentrievers “roll” the clot between the stentriever and the vessel wall.
Images Courtesy of Thomas Liebig, MD, University of Cologne, Cologne - GERMANY
Images Courtesy of Jens Fiehler, MD, University Medical Center Hamburg, Eppendorf - GERMANY
Images Courtesy of Caspar Brekenfield, MD, University of Hamburg, Hamburg - GERMANY
Pulling Vs. Rolling
Intralumenal clot capture surface eliminates wait time
INTRALUMENAL
INTRALUMENAL
LATERAL
LATERAL
Initial TICI Score: 0at 3:10 pm ERIC 6 x 44 Final TICI Score: 3 at 3:24 pm
After 2 Passes
Initial TICI Score: 0at 9:03 pm ERIC 4 x 30 Final TICI Score: 3 at 9:17 pm
After 1 Pass
The ability to select the number of working spheres allows for precise control
Initial TICI Score: 0NIHSS: 5
Partial Recanalisation withERIC 6 x 44 Placed in Occlusion Site
Final TICI Score: 3After 1 Pass
INDICATIONS FOR USE: The ERIC® Retrieval Device is intended for use in the revascularization of acute ischemic stroke caused by the intracranial occlusive vessels of patients who are not eligible for intravenous tissue plasminogen activator, IV tPA, or who fail IV tPA therapy.
MICROVENTION, ERIC, SOFIA and Headway are registered trademarks of MicroVention, Inc. Refer to Instructions for Use, contraindications and warnings for additional information. © 2016 MicroVention, Inc. MM507(i) CHAPLA 8/16
Capturing Clot
100
90
80
70
60
50
40
30
20
10
0
ERIC®
TICI 2a11.1%
TICI 2b30.6%
TICI 352.8%
TICI 2a-3 Revascularization
70
60
50
40
30
20
10
0
ERIC®
mRS 0-233.3%
mRS 325.0%
mRS 0-3 @ 90 Days
Initial clinical experience with the ERIC® device is in line with other peer reviewed, published data on mechanical thrombectomy.
ERIC 3x20
ERIC 4x24
ERIC 4x30
ERIC 6x35
ERIC 6x44
3mm
4mm
4mm
6mm
6mm
203cm
203cm
203cm
203cm
203cm
Distal M2/M3
M1/M2
M1/M2
Proximal M1/ICA
Proximal M1/ICA
PRODUCT PRODUCTCODE
DIAMETER(A)
WORKINGLENGTH
(B)
NUMBEROF
SPHERES
MINIMUMCATHETER ID
(D)
RECOMMENDEDVESSEL
LOCATION
DISTAL TIPLENGTH
(C)
PUSHERLENGTH
(E)
5.0mm
5.0mm
5.0mm
5.0mm
5.0mm
4
4
5
4
5
20mm
24mm
30mm
35mm
44mm
0.017”
0.017”
0.017”
0.017”
0.017”
The MicroVention Stroke System
ER173020
ER174024
ER174030
ER176035
ER176044
A = Diameter
B = Working Length E = Pusher Length
C =Distal TipLength
D =MinimumCatheter
ID
Without The Wait
ERIC is compatible with:
MicroVention, Inc., Worldwide Headquarters, 1311 Valencia Avenue, Tustin, CA 92780 USA Phone: 714.247.8000 Customer Service: 800.990.8368
microvention.com
CHAPLA
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