Radial emission laser fibers – Ringlight®
Ringlight® fibers are intended for the treatment of varicose veins, by endovenous laser. They allow a perfect positioning of the laser beam towards its target therapeutic field: the venous wall.
Designed and developed by LSO Medical, Ringlight® radial emission laser fibers allow optimal energy diffusion for safer and more efficient ablation:
- SMA 905 fiber connector: reference connector
- Si/Si fiber body for optimal energy transmission
- 360° marking along the length of the fibers for an exact dosage of energy and shrinkage speed.
- Fiber tip with radial emission, 360 °: 100 % of the energy is diffused towards the venous wall.
- Encapsulated and rounded fiber tip
– to reduce the risk of vein perforation
– ultrasound and easy to locate by ultrasound - Monitoring Back Reflection, for real-time monitoring of effective delivery at the end of fiber
- Smart card for optimal patient follow-up
- Available in core diameter of 400 μm or 600 μm. High-quality material reduces energy and improves viewing beam transillumination during operation.
The Ringlight_SB® laser fiber is the new generation of LSO Medical radial fiber, compatible with SnakeBack®.
SnakeBack Technology: SnakeBack®® is a tension-free assisted removal system capable of planning, applying and monitoring the energy supply into the vein.
The Ringlight_SB® fibers reflect the design and production quality of Ringlight® fibers.
- Total length: 2.5 m
- Indicator 1: removal of the 6-Fr introducer
- Indicator 2: termination of proceedings
- Centimeter and decimeter markings
Ordering information and technical data
LSO Medical offers you a turnkey solution to launch a thermal endovenous activity.
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a) Ringlight_SB® laser fiber
| Description | Reference | Technical specifications | Compatibility |
|---|---|---|---|
| RINGLIGHT® FIBER PROBE IR_SB 1,8 mm CE 1639 | ORLF000003_SB | Ringlight_SB® Fiber Standard 600 µm, 1.8 mm | Laser : LumeSeal® Introducer 6 Fr |
| RINGLIGHT® FIBER PROBE IRH_SB 1,0 mm CE 1639 | ORLF000005_SB | Ringlight_SB® Fiber Slim 400 µm, 1.0 mm | Laser : LumeSeal® Introducer 4 Fr or Cathlon 16G |
| RINGLIGHT® FIBER PROBE IR_SB 1,8 mm CE 1639 | ORLF000006_SB | Ringlight_SB® Fiber Fused Standard 600 µm, 1.8 mm | Laser : LumeSeal® Introducer 6 Fr |
| RINGLIGHT® FIBER PROBE IRH_SB 1,3 mm CE 1639 | ORLF000007_SB | Ringlight_SB® Fiber Fused Slim 400 µm, 1.3 mm | Laser : LumeSeal® Introducer 4 Fr or Cathlon 16G |
b) Ringlight® laser fiber
| Description | Reference | Technical specifications | Compatibility |
|---|---|---|---|
| RINGLIGHT® FIBER PROBE IR 1,8 mm CE 1639 | ORLF000003 | Ringlight® Fiber Standard 600 µm, 1.8 mm | Laser : Endotherme™ 1470 Introducer 6 Fr |
| RINGLIGHT® FIBER PROBE IRH 1,0 mm CE 1639 | ORLF000005 | Ringlight® Fiber Slim 400 µm, 1.0 mm | Laser : Endotherme™ 1470 Introducer 4 Fr or Cathlon 16G |
| RINGLIGHT® FIBER PROBE IR 1,8 mm CE 1639 | ORLF000007 | Ringlight® Fiber Fused Standard 600 µm, 1.8 mm | Laser : Endotherme™ 1470 Introducer 6 Fr |
| RINGLIGHT® FIBER PROBE IRH 1,3 mm CE 1639 | ORLF000006 | Ringlight® Fiber Fused Slim 400 µm, 1.3 mm | Laser : Endotherme™ 1470 Introducer 4 Fr or Cathlon 16G |
c) Lasers and compatibility
| Description | Reference | Technical specifications | Compatibility |
|---|---|---|---|
| LumeSeal® laser CE 1639 | ENDOV2_SB |
| Compatible with Ringlight_SB® fibers |
| Endotherme™ 1470 laser CE 1639 | PHARAON 1470 |
| Compatible with Ringlight® fibers |
LSO Medical has been able to work with the best suppliers to provide you with all the additional equipment and consumables necessary for the realization of laser procedures:
| Description | Reference | Technical specifications | Compatibility |
|---|---|---|---|
DP 30 Pump – Nouvag 0197 | 4187 |
| Nouvag 6022 / 6022a / 6022b tubing |
| Tubing – Nouvag 0197 | 6022 / 6022a / 6022b | Length: 4 meters | DP 30 Pump – Nouvag |
| Vascular thermal ablation kit 6 Fr – LSO Medical | FR-K66189 | Ringlight® Fiber Standard | |
| Introduction kit 6 Fr – SCW 0197 | INTRO6F03818GS |
| Ringlight® Fiber Standard |
Destinations: vascular surgeons, vascular doctors, pharmacists, biomedical engineers and operating room staff.
Medical equipment Laser: Endotherme™ & LumeSeal_SB®. DM class: IIb. Laser class: 4
Disposables: Ringlight® and Ringlight_SB® Laser Fibers, DM Class: IIa.
1639
Laser Disposable: Ringlight® and Ringlight_SB® fibers are sold sterile. They are sterilized with ethylene oxide. They are designed for single use only. They must not be reused or resterilized.
Endovenous Laser Devices:
Intended Use
The LumeSeal_SB® laser device is used to produce laser energy with controlled parameters (notably wavelength, power, and emission mode) and to deliver it to a compatible output device, such as an endovenous optical fiber, to allow the controlled application of thermal energy within the target vein during endovenous procedures. The device is used under ultrasound guidance and in accordance with the manufacturer’s instructions for use.
Intended Purpose
The LumeSeal_SB® laser device is intended to generate and deliver laser energy for therapeutic purposes, for endovenous use in the coagulation, occlusion, and ablation of the saphenous veins of the lower limbs in patients with chronic venous disease, when endovenous thermal treatment is clinically indicated. The device is intended for use in adult patients by trained healthcare professionals in an appropriate medical environment.
Indications for Use
The LumeSeal_SB® laser device is indicated for use in procedures for the coagulation, occlusion, and endovenous thermal ablation of saphenous veins in patients presenting with venous insufficiency associated with documented venous reflux. The indication is based on a prior clinical and hemodynamic assessment, including an echo-Doppler examination, and on the practitioner’s decision in accordance with current clinical recommendations.
Sterile Consumables:
Intended Use
The Ringlight® / Ringlight_SB® endovenous optical fiber is used to deliver, diffuse, and apply laser energy in a controlled manner within the target vein during endovenous procedures, according to the parameters defined by the compatible laser device. The fiber is used under ultrasound guidance and in accordance with the manufacturer’s instructions for use.
Intended Purpose
The endovenous optical fiber is intended to transmit and diffuse laser energy, generated by a compatible laser device, for therapeutic purposes, for endovenous use in the coagulation, occlusion, and ablation of the saphenous veins of the lower limbs in patients with chronic venous disease, when endovenous thermal treatment is clinically indicated. The endovenous optical fiber is intended for use in adult patients by trained healthcare professionals in an appropriate medical environment.
Indications for Use
The endovenous optical fiber is indicated for use in procedures for the coagulation, occlusion, and endovenous thermal ablation of the saphenous vein in patients presenting with venous insufficiency associated with documented venous reflux. The indication is based on a prior clinical and hemodynamic assessment, including an echo-Doppler examination, and on the practitioner’s decision in accordance with current clinical recommendations.
Benefits: The benefits of endovenous laser treatment are a size reduction or a complete obliteration of the treated varicose veins, and the improvement or even the resolution of venous symptoms. The risk of varicose veins complications will decrease significantly.
Contraindication: LumeSeal_SB® should not be used in the following cases: Patients with thrombi in the venous segment intended for treatment, Patients with an aneurysm in the venous segment intended for treatment, Patients with peripheral vascular diseases with an ankle-arm systolic pressure index below 0.9, Patients with deep vein thrombosis or with a history of deep vein thrombosis, Pregnant patients, Patients with infection on the area to be treated, active herpes or other viral infection, Other contraindications may possibly be indicated by the practitioner at the time of treatment. Read the instructions in the user manual carefully.
Adverse Effects: Based on the analyzed literature, three main categories of adverse effects can be identified for the laser procedure of GSV occlusion: Common adverse effects (incidence < 50%): bruising, pain, and superficial vein thrombosis. Rare adverse effects (incidence < 5% in most studies): deep vein thrombosis, paresthesia, and skin burns. Exceptional adverse effects (fewer than 10 cases reported): persistent paresthesia (lasting more than one year) and pulmonary embolism.
Device Use: Training in the use of LumeSeal® provided by LSO Medical or by individuals authorized by LSO Medical. Carefully read the instructions in the user manual. For the SnakeBack system to comply with the defined requirements, an annual replacement of the wheels and recalibration of the device must be performed, at least once a year. This maintenance must be carried out by a technician that has been officially certified by LSO MEDICAL or by its authorized local distributor. The non-compliance of this rule leads to the cancellation of the manufacturer guarantee.
Endovenous Laser Treatment: Covered by Health Insurance
Manufacturer: LSO Medical, Biocentre A. Fleming, Bât D – 280 rue Salvador Allende – 59120 Loos, France
Distributor and importer: SCW, NOUVAG
Internal reference: 23/04/LSOMEDICAL/PM/001
Version: IM EMB – VA-en