- Condition: Factory New
- Warranty: Lifetime
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Learn more:
- MFR: Sklar Ships from Manufacturer
- MPN: 85-2613
- Phone: (610) 756-7863
Frequently asked questions
Is this sound compatible with standard filiforms?
Yes, this instrument is specifically engineered with a standard 1-56 thread, allowing for seamless attachment of filiforms required for your urethral procedures.
Is the material durable enough for repeated sterilization?
Absolutely. It is manufactured from high-quality stainless steel, designed to withstand the rigors of repeated sterilization cycles without compromising its structural integrity.
Does the handle offer superior control during use?
Yes, the instrument features a specifically designed flat handle. This ergonomic enhancement is engineered to provide the operator with improved grip and greater tactile control during delicate procedures.
What is the specific French size of this sound?
This model is sized at 13 French, which corresponds to a diameter of 4.3mm.
Is the product free of natural rubber latex?
Yes, this urethral sound is not made with natural rubber latex, making it a suitable choice for clinical environments with latex-sensitive patients.
Does this instrument meet professional compliance standards?
Yes, this product is TAA compliant, meeting the rigorous requirements set forth by the Trade Agreements Act.
Is this sound suitable for long-term professional use?
Yes, the instrument is designed as a reusable surgical tool, offering long-term economic value and reliability compared to single-use disposable alternatives.
What is the total length of the instrument?
The Sklar Guyon Urethral Sound has an overall length of 10-3/4 inches, providing the reach necessary for standard sounding procedures.
Does the manufacturer offer any long-term coverage?
Yes, this instrument is backed by a lifetime warranty, reflecting Sklar’s commitment to quality and craftsmanship.
How should this instrument be prepared before its first use?
As this product is delivered non-sterile, it must be properly cleaned and subjected to a validated sterilization cycle by the end-user before it is utilized in any clinical procedure.