- Condition: Factory New
- Warranty: Lifetime
- MFR: Sklar Ships from Manufacturer
- MPN: 66-4980t
- Phone: (610) 756-7863
Buying Sklar Titanium VITREO-RETINAL FCP 23G 2MM T - 66-4980t from MFI Medical
Product details
- Manufacturer part number
- 66-4980t
- MFI SKU
- SKL-66-4980t
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) |
|---|---|---|
| 66-4980tMFI SKU: SKL-66-4980t | Factory NewWarranty: Lifetime | $2,765.51 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
Does this instrument utilize high-grade titanium construction?
Yes, this vitreo-retinal forceps is crafted from high-grade titanium. This material selection is intentional to ensure superior instrument quality, exceptional durability, and the high-level precision required for delicate surgical procedures.
Is this instrument safe for patients with latex sensitivities?
Absolutely. This product is strictly Not Made With Natural Rubber Latex, making it a suitable and safe choice for surgical environments where latex-free compliance is a critical requirement.
Is this tool compliant with TAA standards?
Yes, this Sklar Titanium instrument is fully TAA Compliant. It is designed to meet strict regulatory standards, making it an appropriate choice for facilities or government institutions that require TAA-compliant surgical equipment.
Does it come with any long-term durability guarantees?
The manufacturer stands firmly behind the quality of this instrument. It is supplied as Factory New and is backed by a Lifetime warranty, reflecting the high-grade craftsmanship and long-term durability expected of professional surgical tools.
What sterilization protocol is required before use?
This instrument is supplied as non-sterile. Therefore, it is essential to follow your facility’s standard appropriate sterilization procedures before the instrument is introduced into any surgical field.
Is this model suitable for fine vitreoretinal manipulations?
Yes, it is specifically engineered for precision. The 23G specification and 2MM tip size are optimized for fine vitreoretinal surgical procedures where accuracy and controlled manipulation are paramount.
What is the official Sklar grade for this instrument?
This product features Sklar premium grade construction. This designation signifies that it meets the rigorous manufacturing standards consistent with the Sklar Titanium product line, prioritizing performance for surgical specialists.
Does the purchase include multiple units or just one?
The unit of measure is 1 each. Each package contains a single, high-quality Sklar Titanium vitreo-retinal forceps, ready for your professional surgical use.
Can you confirm the specific model part number?
The manufacturer part number (MPN) for this specific instrument is 66-4980t. You can use this identifier to ensure you are sourcing the exact 23G, 2MM titanium tool required for your surgical tray.
How should this instrument be handled to maintain its precision?
Given its construction from premium-grade titanium, it is designed for repeated use; however, it must always be handled with care to preserve the tip alignment. Always adhere to established medical instrument cleaning and sterilization protocols after every procedure to maintain the integrity of the 23G tip.