Clorox UVDI-360 Advanced UV DISINFECTION ROOM STERILIZATION STERILIZER SANITIZER

$3395.0 Buy It Now or Best Offer
free,30-Day Returns

Seller Store saja137
(1688) 100.0%,

Location: Saint Augustine, Florida
Ships to: US,
Item: 296430946358

Restocking Fee:No
Return shipping will be paid by:Buyer
All returns accepted:Returns Accepted
Item must be returned within:30 Days
Refund will be given as:Money Back
Clorox by UVDI:Clorox by UVDI
Optimum-UV Enlight System:Optimum-UV Enlight System
MPN:Does Not Apply

This unit works as new with very low use. It looks excellent but please see photos for physical details as there are some scuffs. This unit was manufactured by UVDI, makers of UVDI-360 and marketed by Clorox as Optimum-UV Enlight System. The unit is on factory wheels with locks and rolls very smooth.It is powered by a standard 120v wall outlet.Comes with a removable hard casing to protect the 4 UV light bulbs. Delivery will be via a small independent shipping company to ensure a safe arrival.Cost will vary dependent on location with a median price of $400 The following information can be found on the link below. https://www.cloroxpro.com/wp-content/uploads/2018/09/NI-42189_Optimum-UV_Clinical-Lab-Evidence-Booklet.pdf University of Pennsylvania The Optimum-UV® System reduced C. difficile infection (CDI) rates by 25% and averted $134,568–$191,604 annual direct medical costs in Hematology/Oncology units. Principal Investigator: David Pegues, MD, Professor of Medicine, Hospital of the University of Pennsylvania Purpose: To examine the impact of Optimum-UV® System deployment combined with manual surface disinfection with bleach on C. difficile infection rates in Hematology/Oncology units over a 12-month evaluation period. Methods: The Optimum-UV® System was deployed for a 12-month intervention period, in combination with standard manual surface disinfection with bleach. CDI rates were tracked pre- and post-intervention. Results: Deployment of the Optimum-UV® System resulted in a 25% decrease in CDI rates on the study units, as compared to the baseline period. An estimated $134,568 to $191,604 in annual direct medical costs were averted by preventing 21 cases of CDI on the study units. The Optimum-UV® System achieved a >5 log reduction against carbapenem-resistant Enterobacteriaceae (CRE; K. pneumoniae, E. coli, and E. cloacae) in patient rooms. Principal Investigator: Lisa Maragakis, MD, MPH, Senior Director of Infection Prevention and Associate Professor of Medicine, The Johns Hopkins Health System Purpose: To examine Optimum-UV® System efficacy against carbapenem-resistant Enterobacteriaceae (CRE; K. pneumoniae, E. coli and E. cloacae) plated on Formica®. This study is part of a cluster, randomized, two-period crossover trial focused on evaluating MDRO transmission that includes daily patient room cleaning with UV-C in addition to terminal cleaning in Oncology and Solid Organ Transplant units. Methods: UV-C was applied to carbapenem-resistant Enterobacteriaceae plated on Formica® placed on more than 17 high-touch surfaces in a patient room and bathroom. Results: The Optimum-UV® System achieved a >5 log reduction against all three CRE microorganisms tested. No CRE microorganisms grew on 131 out of 133 plates tested following three 5-minute cycles of exposure to UV-C. References: Rock, C.; Curless, M.S.; Nowakowski, E.; Ross, T.; Carson, K.A.; Trexler, P.; Carroll, K.; Maragakis, L.L. UV-C Light Disinfection of Carbapenem-Resistant Enterobacteriaceae from High-Touch Surfaces in a Patient Room and Bathroom. Infect. Control Hosp. Epidemiol. 2016, 1–2. Rock, C.; Curless, M.; Nowakowski, E.; Ross, T.; Carson, K.; Trexler, P.; Carroll, K.; Maragakis, L. UV Light Decontamination of Carbapenem-Resistant Enterobacteriaceae from High Touch Surfaces in a Patient Room and Bathroom. In SHEA (poster presentation); 2016. Optimum-UV® System effectively reduced the presence of multidrug- resistant organisms (MDROs), including C. difficile and methicillin-resistant Staphylococcus aureus (MRSA) in patient rooms. Principal Investigators: Abhishek Deshpande, MD, PhD, Assistant Professor of Medicine, Cleveland Clinic Lerner College of Medicine at Case Western Reserve University Curtis Donskey, MD, Professor of Medicine, Case Western Reserve University and Staff Physician, Infectious Diseases Section, Louis Stokes Cleveland VA Medical Center Purpose: To examine Optimum-UV® System effectiveness against nosocomial pathogens in hospital rooms, including C. difficile and methicillin-resistant Staphylococcus aureus (MRSA). This study is part of a randomized ward-level crossover study on four medical surgical wards during an 8-month period, focused on evaluating C. difficile infection (CDI) rates. This study also included an evaluation of healthcare worker and environmental services staff perceptions. Methods: The Optimum-UV® System was run in isolation rooms on two units in an acute-tertiary care hospital for 6 months. Each patient room was treated for two 5-minute cycles, and the patient bathroom for one 5-minute cycle, for a total of 15 minutes per room. Cultures were collected before and after UV-C treatment to determine the levels of contamination of C. difficile, MRSA, vancomycin-resistant Enterococcus (VRE), and multidrug-resistant gram-negative organisms. Results: The Optimum-UV® System achieved significant reduction in recovery of MRSA and C. difficile during the intervention period, as compared to the preintervention period. MRSA and C. difficile recovery was reduced by 76% (p=0.03) during the intervention, as compared to the preintervention period. References: Deshpande, A.; Hartley, J.; Cadnum, J.; Jencson, A.; Sankar, T. Effectiveness of an Ultraviolet Light Decontamination Device in Reducing Hospital Room Contamination. In SHEA (poster presentation); 2016; p. 549. Deshpande, A.; Hartley, J.; Einloth, C.; Fatica, C.; Donskey, C.; Fraser, T. Perceptions of Healthcare Workers and Environmental Services Staff Regarding Ultraviolet Room Decontamination Devices. In APIC (poster presentation); 2016; p. 251. The Optimum-UV® System effectively kills C. difficile and methicillin- resistant Staphylococcus aureus (MRSA); standardized UV-C device efficacy testing is needed so that different devices can be compared. Principal Investigator: Curtis Donskey, MD, Professor of Medicine, Case Western Reserve University and Staff Physician, Infectious Diseases Section, Louis Stokes Cleveland VA Medical Center Purpose: To determine the impact of variation in UV-C efficacy test methods on log reduction results. Methods: Two UV-C devices, including the Optimum-UV® System, were compared using a single test method for efficacy against MRSA and C. difficile. The Optimum-UV® System was then subjected to further testing whereby one variable at a time was altered to assess the impact on the results, including carrier distance from the lamps, height of the carriers relative to the floor, carrier type, inoculum spread, carrier angle relative to the device and organic load. Results: A >3 log reduction was achieved within 5 minutes for MRSA for both UV devices tested. As expected, log reductions for MRSA and C. difficile changed, depending on the variables tested, including inoculum dispersal, organic load, carrier orientation and carrier height. This study demonstrates the need for industrywide standards for evaluating UV-C device efficacy. References: Cadnum, J.L.; Tomas, M.E.; Sankar, T.; Jencson, A.; Mathew, J.I.; Kundrapu, S.; Donskey, C.J. Effect of Variation in Test Methods on Performance of Ultraviolet-C Radiation Room Decontamination. Infect. Control Hosp. Epidemiol. 2016, 1–6. Cadnum, J.L.; Mana, T.S.C.; Jencson, A.L.; Deshpande, A.; Donskey, C.J. Not All Efficacy Testing Is Created Equal: Effect of Variation in Test Methods on Performance of an Ultraviolet Radiation Room Disinfection Device. In SHEA (poster presentation); 2015. The Optimum-UV® System was associated with a 44% reduction in viral infection incidence among pediatric patients in a long-term care facility. Principal Investigator: Marianne Pavia, MS, BS, CIC, FAPIC, St. Mary’s Hospital for Children Purpose: To examine the impact of the Optimum-UV® System on viral infection incidence in a long-term care pediatric facility. Methods: The Optimum-UV® System was included as an adjunct to standard cleaning protocols for 13 months in a long-term care pediatric facility. UV-C disinfection was focused on the toddler unit, where HAI rates were highest at the time of the intervention. Treatment included patient rooms as well as common areas. Viral respiratory infections were identified using reverse transcription PCR and incidence data werecollected in an electronic medical record and tracked monthly throughout the course of the study. Results: Comparing viral infection incidence rates for the 13-month UV-C deployment period with infection incidence rates for the prior 13-month period, a 44% unadjusted reduction in overall viral infection incidence was found (P-value=0.003), corresponding to an Incidence Rate Ratio [IRR] of 0.56 (95% Confidence Interval [CI]: 0.37-0.84). Patient days per month remained approximately constant throughout the study period, and no other new interventions were implemented during the study period, suggesting that the decrease in viral infection incidence was due solely to the addition of UV-C. References: Pavia, Marianne; Simpser, Edwin; Becker, Melissa; Mainquist, W. Keith; Velez, K. A. The Impact of Ultraviolet-C Technology on Viral Infection Incidence in a Pediatric Long Term Care Facility. Am. J. Infect. 2018, in press. The Optimum-UV® System was associated with a 44% reduction in viral infection incidence among pediatric patients in a long-term care facility. Principal Investigator: Marianne Pavia, MS, BS, CIC, FAPIC, St. Mary’s Hospital for Children Purpose: To examine the impact of the Optimum-UV® System on viral infection incidence in a long-term care pediatric facility. Methods: The Optimum-UV® System was included as an adjunct to standard cleaning protocols for 13 months in a long-term care pediatric facility. UV-C disinfection was focused on the toddler unit, where HAI rates were highest at the time of the intervention. Treatment included patient rooms as well as common areas. Viral respiratory infections were identified using reverse transcription PCR and incidence data werecollected in an electronic medical record and tracked monthly throughout the course of the study. Results: Comparing viral infection incidence rates for the 13-month UV-C deployment period with infection incidence rates for the prior 13-month period, a 44% unadjusted reduction in overall viral infection incidence was found (P-value=0.003), corresponding to an Incidence Rate Ratio [IRR] of 0.56 (95% Confidence Interval [CI]: 0.37-0.84). Patient days per month remained approximately constant throughout the study period, and no other new interventions were implemented during the study period, suggesting that the decrease in viral infection incidence was due solely to the addition of UV-C. References: Pavia, Marianne; Simpser, Edwin; Becker, Melissa; Mainquist, W. Keith; Velez, K. A. The Impact of Ultraviolet-C Technology on Viral Infection Incidence in a Pediatric Long Term Care Facility. Am. J. Infect. 2018, in press.

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