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Cardiocirculatory system devices
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Cardiocirculatory devices - other
Cardiocirculatory devices - other
C99
34 devices
Devices
Cascade
Perflow Medical Ltd.
·
,
IL
Class III
CE/MDR
1000169818
Suspended
Valid to Oct 2027
CE/MDR
170781760
Suspended
Valid to Oct 2027
+1
authorizations
Impella 5.5 with SmartAssist
Abiomed, Inc.
·
,
US
Class III
CE/MDR
aluderm+ LifePad Reanimationshilfe
W.Söhngen GmbH
·
,
DE
Class I
CE/MDR
Cascade 17
Perflow Medical Ltd.
·
,
IL
Class III
CE/MDR
170781760
Suspended
Valid to Oct 2027
CE/MDR
1000169818
Suspended
Valid to Oct 2027
PowerShock
Shunmei̇ Medi̇kal Ve Tibbi̇ Ci̇hazlar Ti̇caret Anoni̇m Şi̇rketi̇
·
,
TR
Class IIb
CE/MDR
Zenix Defibrillation Accessories
Zoll Medical Corporation
·
,
US
Class I
CE/MDR
FibriCheck
Qompium nv
·
,
BE
Class IIa
FDA 510(k)
K232804
Active
Cleared 7 Jun 2024
FDA 510(k)
K173872
Active
Cleared 28 Sep 2018
+2
authorizations
60077
Beurer GmbH
·
,
DE
Class I
CE/MDR
Cascade
Perflow Medical Ltd.
·
,
IL
Class III
CE/MDR
170781760
Suspended
Valid to Oct 2027
CE/MDR
1000169818
Suspended
Valid to Oct 2027
+1
authorizations
FibriCheck
Qompium nv
·
,
BE
Class IIa
CE/MDR
Impella 5.5 with SmartAssist Set
Abiomed, Inc.
·
,
US
Class III
CE/MDD
CE/MDR
Echo-1
Neko Health AB
·
,
SE
Class I
CE/MDR
65302
Beurer GmbH
·
,
DE
Class I
CE/MDR
Occlutech Sizing Balloon
Occlutech GmbH
·
,
DE
Class III
CE/MDR
51030-60-00-01
Expired
Valid to Oct 2026
CE/MDR
51030-61-C0
Active
Valid to Jun 2028
Cascade
Perflow Medical Ltd.
·
,
IL
Class III
CE/MDR
170781760
Suspended
Valid to Oct 2027
CE/MDR
1000169818
Suspended
Valid to Oct 2027
+1
authorizations
Echo-2
Neko Health AB
·
,
SE
Class I
CE/MDR
Impella 5.5 with SmartAssist Set
Abiomed, Inc.
·
,
US
Class III
CE/MDR
Impella CP with SmartAssist Set
Abiomed, Inc.
·
,
US
Class III
CE/MDR
Vitacam
Evondos Oy
·
,
FI
Class IIa
CE/MDD
Impella RP Set
Abiomed, Inc.
·
,
US
Class III
CE/MDR
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