Smith & Nephew TRIVEX™ System Surgical Illuminator REF 7210351, handheld transillumination probe for powered phlebectomy, stainless housing, CE 0123 marked, compatible with TRIVEX console assemblies

Smith & Nephew TRIVEX™ System Surgical Illuminator REF 7210351, handheld transillumination probe for powered phlebectomy, stainless housing, CE 0123 marked, compatible with TRIVEX console assemblies

Condition: Used, great condition. Professionally cleaned; normal cosmetic wear from prior use. Unit is engraved: “REF 7210351”, “SN YN0997”, “US PATENT 5,893,858”, “CE 0123”, and “TRIVEX SYSTEM Illuminator”. No original packaging, accessories, or sterile barrier included.

The Smith & Nephew TRIVEX™ Surgical Illuminator (REF 7210351) is a reusable handheld light probe designed to provide bright, focused transillumination during TRIVEX procedures (transilluminated powered phlebectomy) and related venous surgery. In use, the illuminator is inserted through a small incision to flood the subcutaneous plane with light, enhancing visualization of superficial varicosities while the powered resector addresses targeted tissue. Its compact, robust construction suits operating-room handling and repeated reprocessing when performed per the manufacturer’s IFU. The CE 0123 mark indicates conformity under the notified body 0123 (TÜV SÜD). The engraved U.S. Patent No. 5,893,858 corresponds to technology used in transillumination-assisted venous procedures.

Important: This listing is for the Illuminator instrument only. It requires compatible TRIVEX system components (light source/console, fiber/light cable, and standard surgical accessories) to operate. Item is supplied non-sterile and must be cleaned and sterilized according to the official Instructions for Use (IFU) before clinical use.

Features

• Handheld transillumination probe engineered for the Smith & Nephew TRIVEX™ system
• Bright, directed illumination to enhance visualization of subcutaneous anatomy during venous procedures
• Reusable instrument; supports repeated reprocessing when performed strictly per manufacturer IFU
• Stainless/metallic housing with OR-friendly ergonomics and engraved identifiers for asset tracking
• CE 0123 marking for conformity assessment within the EU/UK (per applicable regulations at time of manufacture)
• Patent reference (US 5,893,858) engraved—corresponds to transillumination surgical technique
• Designed to integrate with TRIVEX light/console assemblies via the specified light/fiber interface
• Low-profile form factor supports small-incision access and atraumatic handling

Applications / Spheres of Application

• Vascular surgery / Phlebology: transilluminated powered phlebectomy (TRIVEX™ technique)
• General/Plastic surgery: illumination-assisted subcutaneous procedures where enhanced visualization is beneficial (per surgeon judgment)
• Teaching environments: demonstration of transillumination anatomy and technique on venous cases

Cross-Referenced Models (Smith & Nephew TRIVEX family)

(Related or system-mate components; verify REF and compatibility.)

• REF 7210351 – TRIVEX Surgical Illuminator (this item)
• TRIVEX Resection Handpiece / Powered Resection Unit (use alongside the illuminator; model varies by generation)
• TRIVEX Light/Console Assembly (required for illumination output; model/REF varies)
• TRIVEX Tumescence Infiltration components (adjunct instruments; model/REF varies)

Cross-references are provided for system context. Always match REF numbers, connection interfaces, and IFU requirements before combining components.

Comparable Products (functional role; other manufacturers)

(For buyers evaluating alternatives with similar clinical purpose; confirm regulatory status, interfaces, and IFU.)

• Transillumination probes used in vein surgery from other vascular platforms (model-specific)
• Illuminating cannulas / lighted retractors providing subcutaneous transillumination (various brands)
• Endoscopic lighted dissectors for illumination of the subdermal plane (procedure- and brand-specific)

Integration & System Use

• System role: Provides the lighted visualization component of the Smith & Nephew TRIVEX™ technique.
• Required mates (not included): Compatible TRIVEX light source/console, appropriate fiber/light cable, and the powered resector and tubing as specified by Smith & Nephew’s IFU.
• Sterilization: Device must be cleaned and sterilized per the manufacturer IFU prior to use. Confirm allowable sterilization cycles and parameters (e.g., steam autoclave, temperature limits).
• Inspection: Prior to any use, inspect lens, distal tip, and connector interface for damage, discoloration, or debris.
• Regulatory markers: CE 0123 (TÜV SÜD) engraved; users are responsible for ensuring ongoing regulatory compliance in their jurisdiction and facility.

Identification & Serialization

• REF (Catalog Number): 7210351
• SN (Serial Number): YN0997 (format observed on engraving; manufacturer-specific coding—may indicate internal batch/sequence. Production date decoding is not confirmed here.)
• Markings on instrument: “REF 7210351”, “SN YN0997”, “US PATENT 5,893,858”, “CE 0123”, “TRIVEX SYSTEM Illuminator”
• UPC/GTIN: Not provided on this unit

What’s Included

• Smith & Nephew TRIVEX™ System Surgical Illuminator, REF 7210351 (single instrument)
• No light source, cables, sterilization tray, drapes, or accessories included

Related

Smith & Nephew TRIVEX illuminator; TRIVEX light probe; surgical transillumination instrument; venous surgery lighted cannula; varicose vein removal illuminator; powered phlebectomy illumination; OR transillumination device; device to illuminate subcutaneous tissue; vascular surgery accessory; CE 0123 surgical instrument; light probe for TRIVEX; surgical illuminator handpiece

Common Requests:

1. “Is the REF 7210351 TRIVEX illuminator compatible with my existing Smith & Nephew TRIVEX console and fiber cable?”
2. “What sterilization cycles are approved for the TRIVEX Surgical Illuminator (steam parameters and cycle limits)?”
3. “Can I use this illuminator with third-party light sources or must it be Smith & Nephew only?”
4. “What inspection/maintenance steps are recommended before and after each case for REF 7210351?”
5. “Does REF 7210351 include the resector or is it strictly the illumination component for TRIVEX procedures?”

Manufacturer Trademarks Disclaimer: Smith & Nephew and TRIVEX are trademarks of Smith & Nephew plc or its affiliates. Any other brand or product names mentioned are the property of their respective owners. Use of these names is for identification and compatibility reference only and does not imply endorsement.

Legal Disclaimer and Terms of Purchase:
The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies. If so, do not bid on or purchase this item unless you are an authorized purchaser.

The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies. If so, do not bid on this item unless you are an authorized purchaser. If the item is subject to FDA regulation, I will verify your status as an authorized purchaser of this item before shipping of the item.

Responsibility of Buyer
By purchasing this item, the buyer assumes full responsibility for the purchase, preparation, inspection, testing, calibration, and use of the item, including ensuring compliance with any applicable regulatory requirements. Medical and dental items must be inspected by a qualified biomedical technician before being placed into use. It is solely the buyer’s responsibility to ensure the item’s safety and suitability for its intended purpose.

If this item is intended for use in conjunction with patient care, diagnosis, or any medical application, it is the buyer’s responsibility to obtain the necessary certifications, licenses, or professional clearances required for such use.

Indemnification and Release of Liability
The buyer agrees that the seller shall not be held responsible or liable for any injuries, damages, or losses, whether incidental or consequential, arising from the purchase, preparation, or use of the item. The buyer further agrees to indemnify, defend, and hold the seller harmless from any claims, actions, or demands, including, without limitation, reasonable legal fees, arising from or related to the buyer’s purchase, preparation, or use of the item.

No Warranty
The seller makes no warranties, express or implied, regarding the condition, functionality, or safety of the item, including but not limited to any implied warranties of merchantability or fitness for a particular purpose. The buyer acknowledges that the item is sold “as is” and “with all faults.” The only exception to this is the seller’s 14-day refund guarantee, which applies only to the purchased item and only for 14 days from the shipping date. No other warranties, guarantees, or remedies apply.

Final Agreement
By purchasing this item, the buyer acknowledges and agrees to the terms of this disclaimer, accepting full responsibility for all aspects of the purchase and use of the item.

P123/B001