The No Rinse Solution
What is XPERIENCE?
XPERIENCE is a no rinse surgical solution, designed to help prevent surgical site infections by rinsing away debris and microorganisms.
The technology deconstructs the biofilm that enters into the solution by removing the metal ions holding the polymer together and destroys the enveloped bacteria. XPERIENCE defends against bacterial recolonisation.
Proven Efficacy against bacteria within the solution
XPERIENCE Advanced Surgical Irrigation is indicated for use in cleansing
and removal of debris, including microorganisms, from wounds.
CONTAINS: Sodium Lauryl Sulfate, Citric Acid, Sodium Citrate, and Water.
*When used per the IFU
†Does not include hydroxyapatite (HA) or fibrin sealants
5 Minute Planktonic Efficacy
Proven Safety
Compatibility
Specifications
WARNINGS/PRECAUTIONS:
· NOT FOR IV USE - This product has been tested as a wound wash only. DO NOT inject.
· External use only.
· The product is single-use and should be applied only once in a 24-hour period.
· Discard any unused solution.
· Do not use if there is a history of allergy to any of the ingredients.
· Avoid eye contact; product may cause ocular irritation.
· Do not use if container is damaged.
· Potential for temporary burning or discomfort may occur.
Do not use with fibrin sealants due to the risk of material degradation.
Application of fibrin sealants in the presence of XPERIENCE Advanced Surgical Irrigation may impact sealant setup.
· Acceptable for use with coated hydroxyapetite (HA) implants. Do not use with solid hydroxyapetite due to the risk of accelerated material degradation.
· If product contacts unintended anatomy or materials, rinse away solution after irrigation.
· The Stryker StrykeFlow II laparoscopic irrigator does not provide adequate pressure to remove debris when used with XPERIENCE Advanced Surgical Irrigation.
· Do not use in the case of substantial tissue loss.
· Use of citrates may result in QT prolongation and other signs of short-term hypocalcemia due to the ability for citrate to chelate ionized calcium.
References
Always read the label and follow the instructions for use This medical device must be administrated by a healthcare professional
*Gupta K, Margques C, Petrova OE, Sauer K. Antimicrobial tolerance of Pseudomonas aeruginosa biofilms is activated during an early developmental stage and requires the two component hybrid sagS.
Journal of Bacteriology. 2013;195(21):4975-4987.
*Leid JG, Willson CJ, Shirtliff ME, et al. The exopolysaccharide
alginate protects Pseudomonas aeruginosa biofilm bacteria from
IFN-mediated macrophage killing. J Immunol. 2005;175(11):7512-7518.
*Williams, D. L. (2019, November 6). Targeting biofilms in translational research, device development, and industrial sectors. Google Books. Retrieved February 28, 2022, from
https://books.google.com/books?id=M8-8DwAAQBAJ
*Data on file: TR-04-21-008, TR-04-21-009
*Data on file: TR-06-19-012, TR-12-19-002
*Data on file: TR-06-19-007
*Data on file: TR-01-21-003, CD-0040
Collectively, infections contribute to significant morbidity, mortality and increased healthcare expenditures.
Proven efficacy against bacteria within the solution
Safety tested showing no irritation
XPERIENCE has been safety tested showing no irritation.