AR-13995N – Arthrex Scorpion Multifire Needle

Arthrex Scorpion Multifire Needle — SKU AR-13995N

The Arthrex Scorpion Multifire Needle is listed under SKU AR-13995N in the Class 1 Inventory catalog, sourced from Arthrex. Its FDA GUDID record identifies it as “Scorpion-multifire needle”, manufactured by ARTHREX,INC. This cross-reference to FDA device data helps confirm you’re ordering the exact item you need.

Product Details

The Arthrex Scorpion® Multifire Needle is designed for repeated suture passage during arthroscopic soft tissue repair. It is compatible with select Arthrex Scorpion® instruments for efficient surgical workflow. Each box contains 5 sterile needles.

When comparing this item to similar products from other manufacturers, use SKU AR-13995N and GTIN 00888867015951 to confirm you’re matching the exact configuration your facility needs.

AR-13995N Ordering & Compatibility

Use this reference number and GTIN 00888867015951 when communicating with purchasing, receiving, or inventory teams, or when submitting a quote request through Class 1 Inventory. FDA records list this item’s commercial-distribution status as In Commercial Distribution. The FDA record also indicates this device is single-use, sterile, though packaging and dating should always be verified on the physical unit received. If you’re not seeing the exact configuration you need, our team can also help source alternatives or discuss options through our buy-back program. You can also look up this GTIN directly in the FDA AccessGUDID database for the full manufacturer record.

If SKU AR-13995N is currently on backorder elsewhere, Class 1 Inventory may already have it in stock or know of a comparable substitute within General Surgical. We work with buyers across Arthrex and other manufacturer lines to keep procurement moving, and we buy back unused surplus inventory as well.

Specifications

• Catalog product name: Arthrex Scorpion Multifire Needle
• SKU / model: AR-13995N
• GTIN / UPC / EAN: 00888867015951
• Brand: Arthrex
• FDA brand name: Arthrex®
• Manufacturer: ARTHREX,INC.
• FDA commercial distribution status: In Commercial Distribution
• FDA record indicates single use: Yes
• FDA record indicates sterile: Yes