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The purpose of this inspection was to determine whether activities and procedures related to your participation in the clinical study "Suprarenal Proximal Cuff Study," Investigational Device Exemption (IDE) G990139, and "UNITE LeMaitre Vascular UniFit Aorto-Uni-liiac Stent Graft Clinical Study," IDE (b)(4), complied with applicable federal regulations

Can I use sterile water instead of bacteriostatic water to reconstitute AHK-Cu

For Mac OS use, additional configuration may be required

Sealed in sterile vials, ready for reconstitution