ROTAPRO™

Rotational Atherectomy System

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ROTAPRO Product Animation video
ROTAPRO Atherectomy System Components
ROTAPRO Product Animation video
ROTAPRO Atherectomy System Components

Easy to Use. Hard on Calcium. ROTAPRO Rotational Atherectomy System is the gold standard mechanism of action on an easy to use platform.

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System Components

 

Console

The ROTAPRO Rotational Atherectomy System console regulates the flow of air to the advancer, controlling burr rotation speed. It also monitors and displays burr rotation speed and rotational atherectomy procedural time. The console may be powered by both nitrogen and compressed air.
  • Vibrant Digital Display – Enhanced feedback and deceleration indicator
  • Streamlined Connections – Quick and easy setup
  • IV Pole Clamp – Installation flexibility
 

Advancer

The ROTAPRO Rotational Atherectomy system features an Advancer which is used to control movement of the burr. The advancer can be purchased individually. 
  • Easy-to-use Controls – Incorporated on the advancer
  • Ergonomic Dynaglide™ Design – Simple system removal
  • Hybrid Harness – Improved cable management
 

Burrs

The ROTAPRO Atherectomy System offers multiple burr size options to achieve predictable lumen size.
 
 
 

Guidewires

ROTAWIRE™ Drive Guidewires are designed specifically for use with the ROTAPRO Rotational Atherectomy System.
  • Steerability – able to navigate calcified lesions with 1:1 torque through tortuous anatomy, providing access for ROTAPRO Rotational Atherectomy System
  • Tip Design - .014” platinum coil to provide visibility during Rotation atherectomy
  • Core Wire – one-piece core wire with Asahi technology, transmits torque for predictable steering

Choose between the  ROTAWIRE™ Drive Floppy or  ROTAWIRE™ Drive Extra Support models depending on procedure requirements.

 

 

ROTAGLIDE™

ROTAGLIDE™

ROTAGLIDE is a lipid based emulsion designed to lubricate the ROTAPRO System.*

  • Reduces friction and improves tactile feel
  • Reduces heat build-up around the ROTAPRO burr
  • Reduces sudden drops in RPMs caused by lesion feedback

*Contraindicated if patient is allergic to eggs or olive oil

 

Ordering Information

 

ROTAPRO System Console

Order Number Model/ Description
H749 3930901 0 ROTAPRO Console Kit
 

ROTAPRO Pre-Connected Burr and Advancing Device

Order Number Model/Description Burr Size Length Maximum Diameter
H749 39467125 0 ROTAPRO Pre-Connected Burr and Advancing Device 1.25 mm 135 cm 0.58 inch
H749 39467150 0 ROTAPRO Pre-Connected Burr and Advancing Device 1.5 mm 135 cm 0.58 inch
H749 39467175 0 ROTAPRO Pre-Connected Burr and Advancing Device 1.75 mm 135 cm 0.58 inch
H749 39467200 0 ROTAPRO Pre-Connected Burr and Advancing Device 2.0 mm 135 cm 0.58 inch
H749 39467215 0 ROTAPRO Pre-Connected Burr and Advancing Device 2.15 mm 135 cm 0.58 inch
H749 39467225 0 ROTAPRO Pre-Connected Burr and Advancing Device 2.25 mm 135 cm 0.58 inch
H749 39467238 0 ROTAPRO Pre-Connected Burr and Advancing Device 2.38 mm 135 cm 0.58 inch
H749 39467250 0 ROTAPRO Pre-Connected Burr and Advancing Device 2.5 mm 135 cm 0.58 inch
 

ROTAWIRE™ Drive Guidewire

Order Number Model/ Description Length Tip Length Flexibility Spring Tip Diameter Maximum Diameter Quantity
H749 3946300 5 ROTAWIRE™ Drive Extra Support Guide Wire with WireClip™ Torquer 330 cm 2.8 cm Stiff 0.009 inch 0.014 inch Box of 5
H749 3946200 5 ROTAWIRE™ Drive Floppy Guide Wire with WireClip™  Torquer 330 cm 2.2 cm Flexible 0.009 inch 0.014 inch Box of 5
 

Accessories

Order Number Model/Description Quantity
H802 21600003 1 Replacement Braided Air Hose Single
H749 3936801 0 Replacement Power Cord – North America Single
H802 1590101 1 Regulator Kit – North America Single
H802 22196003 2 WireClip Torquer Box of 5
 

ROTAGLIDE™ Lubricant

Order Number Model/Description Quantity
H749 23548-001 62 ROTAGLIDE Lubricant Mixture 20 cc vials Box of 6
 

Reimbursement

The C-code used for this product is C1724, catheter, transluminal atherectomy, rotational. The ROTAWIRE™ Drive Guidewire C-code is C1769. C-codes are used for hospital outpatient device reporting for Medicare and some private payers. 

Note: Boston Scientific is not responsible for the correct use of codes on submitted claims; this information does not constitute reimbursement or legal advice.

 
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