Boston Scientific Flexiva Pulse ID 242 M006L8406910 High-Power Laser Fiber 3m

SKU: BOSTM006L8406910LON
$175.00
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Boston Scientific Flexiva Pulse ID 242 High-Power Laser Fiber

The Boston Scientific Flexiva Pulse ID 242 is a high-power, single-use laser fiber designed to transmit Ho:YAG laser energy during urological procedures.

Its flexible 242-micron fiber and reinforced construction are designed to support high-frequency energy delivery while navigating through a deflected ureteroscope. The integrated identification technology is designed for compatibility with supported RFID-enabled Lumenis laser consoles.

Product Specifications

  • Manufacturer: Boston Scientific Corporation

  • Brand: Flexiva Pulse ID

  • Model/UPN: M006L8406910

  • GTIN: 08714729978671

  • Fiber Size: 242 µm

  • Fiber Length: 3 meters

  • Device Type: High-power surgical laser fiber

  • Laser Type: Ho:YAG

  • Console Compatibility: Supported RFID-enabled Lumenis laser systems

  • Package Quantity: One

  • Single Use: Yes

  • Prescription Device: Yes

  • FDA Device Class: Class II

Key Features

  • Designed for high-power and high-frequency Ho:YAG laser systems

  • Flexible 242-micron fiber profile

  • Designed to deliver energy through a deflected ureteroscope

  • Proprietary fiber coating supports flexibility and durability

  • Integrated identification technology for compatible Lumenis consoles

  • Individually packaged for single-use applications

Condition and Sterility

New in the manufacturer’s original packaging.

This product was supplied sterile and is intended for single use. Sterility is maintained only when the original sterile barrier remains unopened and undamaged and the product is within its labeled expiration range.

Do not use if the packaging is opened, damaged, or otherwise compromised. Do not reuse, reprocess, or resterilize.

Available expiration ranges are managed through the product options shown on this listing. Please select the appropriate available option when ordering.

Purchaser is responsible for confirming compatibility with the intended laser console before use.

Prescription device. Sale and use are subject to applicable federal, state, and local requirements. Intended for purchase and use by appropriately licensed healthcare facilities and professionals.

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