- Condition: Factory New
- Warranty: Lifetime
- MFR: Sklar Ships from Manufacturer
- MPN: 70-1084
- Phone: (610) 756-7863
Buying Sklar Thudichum (Goldsmith) Nasal Speculum - 70-1084 from MFI Medical
Product details
- Manufacturer part number
- 70-1084
- MFI SKU
- SKL-70-1084
Supplier, condition & warranty
- Supplier
- MFI Medical Equipment, Inc.
- Brand
- Sklar
- Condition
- Factory New
- Listed warranty
- Lifetime
MFI Medical is an authorized distributor for all new Sklar items we sell. Any included warranty on a new item is provided directly by the manufacturer. MFI Medical is available to assist with manufacturer warranty claims.
Healthcare purchasing support: MFI Medical provides formal quotations, accepts purchase orders, and offers payment terms to approved customers. W-9 and vendor onboarding information and purchase order and payment instructions are available online.
Purchasing and warranty assistance: MFI Medical: (800) 633-1558. Contact MFI Medical · Warranty policy. Manufacturer product support: (610) 756-7863.
Price & shipping
| MPN | Condition & warranty | Item price (USD) |
|---|---|---|
| 70-1084MFI SKU: SKL-70-1084 | Factory NewWarranty: Lifetime | $40.05 Free shipping* |
*Free standard shipping to the contiguous U.S. on eligible orders of US$35 or more. Other destinations and upgraded services cost extra. Shipping policy
Frequently asked questions
Is this nasal speculum built for professional clinical use?
Yes, the Sklar Thudichum (Goldsmith) Nasal Speculum is a professional-grade surgical instrument designed for hospitals, surgery centers, and ENT private practices. It is constructed from high-quality stainless steel to provide the durability and reliability required for frequent clinical use.
Does this tool offer high-level clinical precision?
Absolutely. It features a specialized U-shaped design that allows for the precise widening of the nasal cavity. This enhances visibility, making it an essential tool for procedures such as:
- Septoplasties
- Removal of foreign objects
- General nasal examinations
Can this be reused between different patients?
Yes, this is a reusable instrument. It is built from durable stainless steel, allowing it to withstand regular cycles in standard sterilization equipment, making it a long-term investment for your facility.
Is this product safe for patients with latex allergies?
Yes, the speculum is completely latex-free. It is crafted without the use of natural rubber latex, ensuring safety for both patients and healthcare staff who may have sensitivities.
What are the specific blade dimensions for this model?
This unit is the Size #4 model, which features blade dimensions of:
- Width: 9mm
- Length: 17mm
These dimensions are optimized to balance effective nasal cavity widening with patient comfort.
Does this meet official government procurement standards?
Yes, the instrument is TAA (Trade Agreements Act) Compliant. This certification ensures that it meets the necessary standards for government and institutional procurement processes.
How should I maintain the steel finish of this tool?
To maintain the longevity of the stainless steel, it is recommended to pair this instrument with standard sterilization equipment. Proper cleaning and sterilization protocols after each use will help preserve the instrument’s professional-grade finish and structural integrity.
Is the design comfortable for patient insertion?
The instrument features a refined, U-shaped “hairpin” design with rounded corners on the blades. This design is specifically engineered to gently widen the nostrils while maximizing patient comfort during the examination process.
Is this instrument considered a high-quality surgical tool?
Sklar is a recognized brand in surgical instrumentation. This speculum is factory new and manufactured to meet strict surgical requirements, backed by a lifetime warranty against defects, confirming its status as a high-quality, durable piece of medical equipment.
Is this instrument delivered in a sterile state?
No, the Sklar Thudichum Nasal Speculum is provided in a non-sterile state. It must be subjected to your facility’s validated sterilization process before its first use and between every subsequent clinical application.