Smith & Nephew, Inc.
DURAFIBER AG
SKU K103793UPC FRO
In Stock
—
FDA 510(k) Cleared (K103793)
1
Free shipping on orders over $99 · 30-day returns
Smith & Nephew, Inc.
Free shipping on orders over $99 · 30-day returns
DURAFIBER AG is an FDA 510(k)-cleared medical device (K103793) manufactured by Smith & Nephew, Inc.. This device is classified under the Unknown specialty. FDA Device Class U. FDA clearance granted on May 1, 2011.
Ansell
SKU MSC846624
Princeton BioMeditech Corp.
SKU K014192
Ohmeda Medical
SKU K871399
Insulet Corporation
SKU K182630