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CEDAR™ Endovenous Radiofrequency System

The CEDAR Endovenous Radiofrequency Ablation System* is designed for the treatment of patients with superficial vein reflux, and includes the CEDAR Generator and CEDAR Catheters.

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Why choose CEDAR RFA System

Intuitive

CEDAR provides a seamless RFA procedure experience. Designed for intuitive set up, the generator’s touch screen displays real-time parameters and key procedure information, and provides auditory feedback during treatment.

Available with 3 cm or 7 cm heating coil treatment lengths, the catheter features clear markings and one-button activation.

Reliable

Designed for efficient procedures. The CEDAR catheter’s coil consistently heats to 120° C for effective destruction of the endothelial cells to induce venous spasm and closure of the targeted segment. You can count on consistent product supply and robust support services from a trusted partner. 

Effective

CEDAR RFA System is backed by Level 1 clinical evidence, which demonstrated 97.78% closure of the GVS, 0 safety incidents, and -3.7+3.97 VCSS Score change.1

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1. Shang T, Zhu YF, Jiang JS, He J, Yang J, Lu T, et al. A multicenter randomized controlled trial evaluating a new radiofrequency ablation system in the treatment of primary great saphenous vein incompetence: Six-month results of the ACOART RF CLOSURE study. Phlebology. 2026. doi:10.1177/02683555261426651

Clinical data

CEDAR RFA clinical trial outcomes

A multicenter, randomized controlled trial evaluating a new radiofrequency ablation system in the treatment of primary great saphenous vein incompetence: Six-month results of the ACOART RF CLOSURE study1

Study Overview

  • Multicenter, randomized controlled trial evaluating the CEDAR RFA system versus ClosureFast™
  • 188 patients with primary great saphenous vein (GSV) incompetence enrolled across 5 vascular centers
  • Primary endpoint: total GSV occlusion at 6 months
  • Secondary endpoints: device success, technical success, patient‑reported outcomes (AVVQ, VCSS), and safety

Key Results

Effectiveness

  • Complete GSV occlusion at 6 months:
    • CEDAR: 97.78%
    • ClosureFast: 98.86%
  • Device success: 100% for both systems
  • Immediate technical success: 100% for both systems
  • Patient outcomes: Significant and comparable improvement in AVVQ and VCSS scores in both groups
  • Large‑diameter vein performance:
    • Patients with GSV ≥12 mm: 100% occlusion at 6 months for both devices

Safety

  • Overall adverse event rates comparable between systems
  • No device‑related adverse events or serious adverse events (SAEs) recorded

1. Shang T, Zhu YF, Jiang JS, He J, Yang J, Lu T, et al. A multicenter randomized controlled trial evaluating a new radiofrequency ablation system in the treatment of primary great saphenous vein incompetence: Six-month results of the ACOART RF CLOSURE study. Phlebology. 2026. doi:10.1177/02683555261426651

Technical information

CEDAR Endovenous RFA Catheter specifications 

Model 

ERA-C70-US 

ERA-C30-US  

Introducer sheath (min. ID size) 

7F (2.3 mm) 

7F (2.3 mm)  

Insertable length 

60 cm 

60 cm  

Heating element diameter 

2.15 mm 

2.15 mm  

Heating element length 

7 cm 

3 cm  

Max power setting 

40W 

18W  

Default target temperature setting 

120°C 

120°C  

Compatible guidewire 

0.025 in 

0.025 in  

CEDAR Endovenous RFA Generator specifications 

ModelERA-G5-US 
Input110–230 VAC, 50/60 Hz, 120 VA  
Height11.0 in 
Width14.2 in 
Depth7.6 in 
Weight12.1 lbs  

Ordering information

Product NameUPN
CEDAR™ Endovenous Radiofrequency Ablation Catheter (3 cm)ERA-C30-US
CEDAR Endovenous Radiofrequency Ablation Catheter (7 cm)ERA-C70-US
Endovenous Radiofrequency GeneratorERA-G5-US

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*CEDAR™ Endovenous Radiofrequency Ablation System includes the CEDAR Endovenous Radiofrequency Catheter and Endovenous Radiofrequency Generator

CEDAR RFA System manufactured by Acotec Scientific Co., Ltd. and distributed exclusively in the U.S. by Boston Scientific.