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EKOS™

EKOS™

The EKOS™ Endovascular System is used for ultrasound-assisted, catheter-directed thrombolysis to quickly and safely dissolve pulmonary embolism (PE). Minimally invasive, EKOS™ leverages the power of targeted ultrasonic waves to thin and separate fibrin strands and accelerates lytic dispersion deeper into the clot.

Treatment Zone (cm):
Working Length (cm):
Model:
Qty:

H74939590106060

Qty : 1

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EKOS ENDOVASCULAR DEVICE 106X6CM
Qty : 1
Treatment Zone (cm) : 6.0
Working Length (cm) : 106.0
Model : Catheter
GTIN : 00191506010942
EKOS ENDOVASCULAR DEVICE 106X12CM
Qty : 1
Treatment Zone (cm) : 12.0
Working Length (cm) : 106.0
Model : Catheter
GTIN : 00191506010959
EKOS ENDOVASCULAR DEVICE 106X18CM
Qty : 1
Treatment Zone (cm) : 18.0
Working Length (cm) : 106.0
Model : Catheter
GTIN : 00191506010966
EKOS ENDOVASCULAR DEVICE 106X24CM
Qty : 1
Treatment Zone (cm) : 24.0
Working Length (cm) : 106.0
Model : Catheter
GTIN : 00191506010973
EKOS ENDOVASCULAR DEVICE 106X30CM
Qty : 1
Treatment Zone (cm) : 30.0
Working Length (cm) : 106.0
Model : Catheter
GTIN : 00191506010980
EKOS ENDOVASCULAR DEVICE 106X40CM
Qty : 1
Treatment Zone (cm) : 40.0
Working Length (cm) : 106.0
Model : Catheter
GTIN : 00191506010997
EKOS ENDOVASCULAR DEVICE 106X50CM
Qty : 1
Treatment Zone (cm) : 50.0
Working Length (cm) : 106.0
Model : Catheter
GTIN : 00191506011000
EKOS ENDOVASCULAR DEVICE 135X12CM
Qty : 1
Treatment Zone (cm) : 12.0
Working Length (cm) : 135.0
Model : Catheter
GTIN : 00191506011017
EKOS ENDOVASCULAR DEVICE 135X30CM
Qty : 1
Treatment Zone (cm) : 30.0
Working Length (cm) : 135.0
Model : Catheter
GTIN : 00191506011024
EKOS ENDOVASCULAR DEVICE 135X40CM
Qty : 1
Treatment Zone (cm) : 40.0
Working Length (cm) : 135.0
Model : Catheter
GTIN : 00191506011031
EKOS ENDOVASCULAR DEVICE 135X50CM
Qty : 1
Treatment Zone (cm) : 50.0
Working Length (cm) : 135.0
Model : Catheter
GTIN : 00191506011048
EKOS CONTROL UNIT 4.0
Qty : 1
Model : Control Unit 4.0
GTIN : 00191506011277
EKOS CONTROL UNIT 4.0 CIC
Qty : 1
Model : Connector Interface Cable (CIC)
GTIN : 00191506024017
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EKOS ENDOVASCULAR DEVICE 106X6CM

H74939590106060
Qty 1
Treatment Zone (cm) 6.0
Working Length (cm) 106.0
Model Catheter
GTIN 00191506010942

EKOS ENDOVASCULAR DEVICE 106X12CM

H74939590106120
Qty 1
Treatment Zone (cm) 12.0
Working Length (cm) 106.0
Model Catheter
GTIN 00191506010959

EKOS ENDOVASCULAR DEVICE 106X18CM

H74939590106180
Qty 1
Treatment Zone (cm) 18.0
Working Length (cm) 106.0
Model Catheter
GTIN 00191506010966

EKOS ENDOVASCULAR DEVICE 106X24CM

H74939590106240
Qty 1
Treatment Zone (cm) 24.0
Working Length (cm) 106.0
Model Catheter
GTIN 00191506010973

EKOS ENDOVASCULAR DEVICE 106X30CM

H74939590106300
Qty 1
Treatment Zone (cm) 30.0
Working Length (cm) 106.0
Model Catheter
GTIN 00191506010980

EKOS ENDOVASCULAR DEVICE 106X40CM

H74939590106400
Qty 1
Treatment Zone (cm) 40.0
Working Length (cm) 106.0
Model Catheter
GTIN 00191506010997

EKOS ENDOVASCULAR DEVICE 106X50CM

H74939590106500
Qty 1
Treatment Zone (cm) 50.0
Working Length (cm) 106.0
Model Catheter
GTIN 00191506011000

EKOS ENDOVASCULAR DEVICE 135X12CM

H74939590135120
Qty 1
Treatment Zone (cm) 12.0
Working Length (cm) 135.0
Model Catheter
GTIN 00191506011017

EKOS ENDOVASCULAR DEVICE 135X30CM

H74939590135300
Qty 1
Treatment Zone (cm) 30.0
Working Length (cm) 135.0
Model Catheter
GTIN 00191506011024

EKOS ENDOVASCULAR DEVICE 135X40CM

H74939590135400
Qty 1
Treatment Zone (cm) 40.0
Working Length (cm) 135.0
Model Catheter
GTIN 00191506011031

EKOS ENDOVASCULAR DEVICE 135X50CM

H74939590135500
Qty 1
Treatment Zone (cm) 50.0
Working Length (cm) 135.0
Model Catheter
GTIN 00191506011048

EKOS CONTROL UNIT 4.0

H7493959340010
Qty 1
Model Control Unit 4.0
GTIN 00191506011277

EKOS CONTROL UNIT 4.0 CIC

H7493966540060
Qty 1
Model Connector Interface Cable (CIC)
GTIN 00191506024017

 

All images taken by Boston Scientific. All trademarks are the property of their respective owners. CAUTION: The law restricts these devices to sale by or on the order of a physician. Indications, contraindications, warnings and instructions for use can be found in the product labelling supplied with each device. Information for use only in countries with applicable health authority registrations. This material not intended for use in France. Products shown for INFORMATION purposes only and may not be approved or for sale in certain countries. Please check availability with your local sales representative or customer service...