EndoWrist 471296 – LARGE SUTURE CUT NEEDLE DRIVER

About the Intuitive EndoWrist 471296 – LARGE SUTURE CUT NEEDLE DRIVER

The EndoWrist 471296 – LARGE SUTURE CUT NEEDLE DRIVER is listed under SKU 471296 in the Class 1 Inventory catalog, sourced from Intuitive. Its FDA GUDID record identifies it as “Large suture cut needle driver”, manufactured by INTUITIVE SURGICAL, INC. This cross-reference to FDA device data helps confirm you’re ordering the exact item you need.

Product Details

The Intuitive Surgical da Vinci® Xi Large SutureCut™ Needle Driver combines precise needle handling with integrated suture cutting for efficient robotic-assisted suturing. EndoWrist® articulation provides enhanced control and dexterity. The instrument is validated for up to 15 uses.

Because it’s cataloged under SKU 471296, this listing gives buyers a consistent way to reorder the exact same configuration every time, rather than relying on the product name alone, which can vary slightly across price lists and manufacturer updates.

471296 Ordering & Compatibility

For reordering and inventory matching, use the SKU and GTIN shown on this page. FDA records list this item’s commercial-distribution status as In Commercial Distribution. Reach out if you need help confirming compatibility with your existing equipment or want to explore backorder alternatives. You can also look up this GTIN directly in the FDA AccessGUDID database for the full manufacturer record.

If SKU 471296 is currently on backorder elsewhere, Class 1 Inventory may already have it in stock or know of a comparable substitute within Sutures. We work with buyers across Intuitive and other manufacturer lines to keep procurement moving, and we buy back unused surplus inventory as well.

Specifications

• Catalog product name: EndoWrist 471296 – LARGE SUTURE CUT NEEDLE DRIVER
• SKU / model: 471296
• GTIN / UPC / EAN: 00886874121504
• Brand: Intuitive
• FDA brand name: EndoWrist
• Manufacturer: INTUITIVE SURGICAL, INC.
• FDA commercial distribution status: In Commercial Distribution
• FDA record indicates single use: No
• FDA record indicates sterile: No