NUS-109 – Stryker Adherus AutoSpray ET Dural Sealant

About the Stryker Adherus AutoSpray ET Dural Sealant — SKU NUS-109

SKU NUS-109 corresponds to the Stryker Adherus AutoSpray ET Dural Sealant from Stryker, manufactured by STRYKER CORPORATION. According to its FDA GUDID device record, this item is described as “Adherus autospray et dural sealant”. We include this FDA-sourced identification alongside the standard catalog details so purchasing and receiving teams can verify the exact device before it ships.

Product Details

The Stryker Adherus™ AutoSpray ET Dural Sealant is designed to reinforce dural closures and help prevent cerebrospinal fluid leaks. It forms a flexible hydrogel barrier over surgical repair sites. Each package contains one sealant system.

When comparing this item to similar products from other manufacturers, use SKU NUS-109 and GTIN 00897146002025 to confirm you’re matching the exact configuration your facility needs.

NUS-109 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. The FDA record also indicates this device is single-use, sterile, though packaging and dating should always be verified on the physical unit received. 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 NUS-109 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 Stryker and other manufacturer lines to keep procurement moving, and we buy back unused surplus inventory as well.

Specifications

• Catalog product name: Stryker Adherus AutoSpray ET Dural Sealant
• SKU / model: NUS-109
• GTIN / UPC / EAN: 00897146002025
• Brand: Stryker
• FDA brand name: Adherus
• Manufacturer: STRYKER CORPORATION
• FDA commercial distribution status: In Commercial Distribution
• FDA record indicates single use: Yes
• FDA record indicates sterile: Yes