07ALaser Energy · Vascular SurgeryFLAGSHIP
NOVACURE Semiconductor Laser Treatment System
Partner-supplied diode laser source for 1470 nm endovenous laser workflows.
Classification
Class III
NMPA Reg.
Guo Xie Zhu Zhun 20253011190
A partner-supplied diode laser source used with VEMERIX's 1470 nm endovenous laser energy platform, which is built around Medison's NMPA-registered single-use medical laser fiber. Current product media identify NOVACURE 1470 nm and NOVACURE-Dual 980 nm + 1470 nm configurations for varicose-vein treatment.
KEY FEATURES
What makes it work.
- Partner-supplied laser source for endovenous varicose-vein workflows
- 1470 nm configuration plus NOVACURE-Dual 980 nm + 1470 nm option shown in product media
- Touchscreen workflow with preset mode and parameter controls
- Pairs with Medison single-use medical laser fibers and compatible accessories
APPLICATIONS
Where it's used.
- Endovenous laser ablation workflows for varicose veins
SPECIFICATIONS
Technical specifications.
Classification
NMPA Class III medical device
NMPA registration
Guo Xie Zhu Zhun 20253011190
Registration holder
Guangdong Yunshang (white-label production)
Configurations
NOVACURE 1470 nm · NOVACURE-Dual 980 nm + 1470 nm
Partner consumable
Medison NMPA-registered single-use medical laser fiber (Lu Mech Reg. 20192010517)
CE / FDA
Listed as available in supplier product table
FROM VEMERIX INSIGHTS
Market analysis behind this product
Buyer Guide
Which Laser-Safety File Belongs With a 1470 nm Fiber Shipment
An incoming-inspection and supplier-qualification guide for international medical-device distributors, hospital clinical-engineering leads, and OEM buyers evaluating Chinese 1470 nm endovenous laser fiber shipments, partner-supplied generators, IEC 60601-2-22 editions, Laser Notice 56, and GB 9706.222 on 17 September 2026.
September 17, 2026 · 18 min read
Regulatory Guide
Which Part Is the Device? How Public Registers Separate Endovenous Laser Fibers, Generators and Kits (2026)
Buyers say ‘the laser.’ Certificates name a fiber, a generator, or a vague system.
August 24, 2026 · 39 min read
Buyer Guide
What the FDA MAUDE and Recall Record Reveals About Endovenous Laser Fiber Failures: A Post-Market Evidence Map for Vascular Procurement and Supplier Screening
An original FDA surveillance analysis of 186 laser fiber clearances, 68 recalls, and 114 MAUDE adverse-event reports (2023–2026) translated into vascular incoming-acceptance criteria and supplier-qualification tests.
August 10, 2026 · 15 min read
Buyer Guide
1470 nm Endovenous Laser System Price & Total Cost of Ownership: A Console, Fiber, Accessory and Per-Procedure Cost Framework
A B2B buyer guide and total-cost-of-ownership framework for clinical directors, distributors, and procurement teams evaluating 1470 nm endovenous laser ablation (EVLA) systems.
August 5, 2026 · 32 min read
Regulatory Guide
Registering and Distributing a Single-Use Endovenous Laser Fiber: A US (FDA 510(k)), EU (MDR) and China (NMPA) Registration and Market-Entry Evidence Pack
A market-entry regulatory guide for medical device distributors and regulatory leads preparing US FDA 510(k), EU MDR Class IIb, and China NMPA registration evidence packs for single-use 1470 nm medical laser fibers.
August 3, 2026 · 18 min read
Market Analysis
From Stripping to Light: The Global Shift to Endovenous Ablation for Varicose Veins
How the standard of care moved from open vein stripping to minimally-invasive endovenous treatment — and why the recurring single-use consumable, not the laser console, is the strategic prize for device makers and distributors.
June 21, 2026 · 25 min read
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