Gigli Wire Saw

Clinical Utility: Specialized orthopedic osteosynthesis implant designed for trauma & reconstructive orthopedics.
Working Profile: Anatomically pre-contoured low-profile geometry engineered to eliminate soft tissue impingement.
Metallurgy & Finish: Medical-grade German Stainless Steel; electropolished satin finish to eliminate operating microscope glare.
Reprocessing Integrity: Fully validated for repeated high-temperature steam autoclaving (134°C / 273°F).
Quality Standards: Compliant with ASTM F899, ISO 13485, and CE MDR medical device manufacturing standards.

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OEM & International Cross-Reference Equivalents

UNIVERSAL NOMENCLATURE EU MDR 2017/745 & US FDA GUDID Classification

EMDN (EUDAMED): L0313

GENERAL SURGERY INSTRUMENTS, REUSABLE

GMDN Code: 32886

Wire holding/twisting forceps

Manufacturer / Benchmark	Catalog Number (REF)	Specification Match
Aesculap	`FH414`	Exact Pattern Match
Medline	`PF31031`	Exact Pattern Match
RZ-Medizintechnik	`290-101-300`	Exact Pattern Match

Notice of Nominative Fair Use: All manufacturer names, trademarks, symbols, and catalog part numbers are referenced solely for comparative identification, cross-reference, and equipment compatibility guidance. SurgiValley is an independent surgical manufacturer and is not affiliated with, sponsored by, or endorsed by any of the respective trademark owners.

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SKU: 023210006

Categorias: Serras

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Surgical Engineering & Procedural Architecture

The Gigli Wire Saw is manufactured to the highest clinical specifications, delivering superior tactile sensitivity, mechanical durability, and ergonomic balance for specialized surgical interventions. Precision-machined from certified medical-grade german stainless steel, each instrument undergoes rigorous heat treatment and multi-stage manual finishing at the workshop bench.

Key Performance Specifications

Specification	Clinical Parameter
Instrument Category	Orthopedic Osteosynthesis Implant
Primary Specialty	Trauma & Reconstructive Orthopedics
Material Metallurgy	German Stainless Steel (Corrosion-Resistant)
Sterilization Protocol	Steam Autoclave (134°C / 273°F) / ETO / Cold Soak
Manufacturing Standard	DIN EN ISO 13485 / ASTM F899 / CE MDR Class I

Surgical Instructions for Use & Autoclave Reprocessing

Prior to initial operative use and following every surgical procedure, this instrument must be reprocessed in strict compliance with ANSI/AAMI ST79 guidelines:

Point-of-Use Pre-Treatment: Rinse immediately following surgery to prevent blood and surgical debris from drying on working edges and hinges.
Ultrasonic Cleaning: Fully immerse in an enzymatic detergent solution (neutral pH 7.0–8.5) and cycle in an ultrasonic bath for 10–15 minutes.
Lubrication: Apply medical-grade, water-soluble instrument lubricant (surgical milk) to all articulating joints and hinge assemblies.
Steam Sterilization: Dynamic-air-removal (pre-vacuum) autoclave cycle at 134°C (273°F) for a minimum 4-minute exposure, followed by a 30-minute drying phase.