Request For Quotation Acquisition Of Other Inventories

The Disinfectant (Concentrate) Must Contain Polyhexamethylene Guanidine Hydrochloride (Phmg) No More Than 2.0%, Benzalkonium Chloride No More Than 4.5% (Qac), As Well As A Surfactant, Complexing Agent And Water. The Product Should Not Contain Aldehydes, Chlorine, Peroxide, Or Acids. Ph Should Be 7.5-10.5. The Product Must Have Bactericidal, Tuberculocidal (Against The Pathogen M. Terrae), Virucidal, And Fungicidal Activity. The Product Must Be Approved For Use For: Disinfection And Cleaning Of Indoor Surfaces; Disinfection (Combined And Not Combined With Pso) Of Medical Devices And Medical Equipment; Disinfection Combined With Pso Of Flexible And Rigid Endoscopes. Shelf Life Is At Least 5 Years, Working Solutions Are At Least 15 Days. The Product Must Be Accompanied By Indicator Strips For Iec Express Control (Up To 100 Liters Of Concentrate 1 Package, Then For Every 100 Liters Of Concentrate 1 Package). Euro Bottle With A Volume Of At Least 1 Liter., As A Disinfectant, The Composition Should Include The Sodium Salt Of Dichloroisocyanuric Acid - 85%, As Well As Sodium Bicarbonate, Adipic Acid And Sulfanol. The Product Should Be Produced In The Form Of Tablets Weighing 3.2 ± 0.35 G. When 1 Tablet Is Dissolved In Water, At Least 1.3-1.7 (41.0-45.0%) Active Chlorine Should Be Released. The Product Must Have Bactericidal (Pathogens Of Especially Dangerous Infections - Plague, Cholera, Tularemia), Virucidal, Tuberculocidal And Sporicidal Activity (Pathogens Of Anthrax), And Also Have The Ability To Decontaminate Objects Contaminated With Dna/Rna Amplicons. The Product Must Be Approved For: - Disinfection Of Indoor Surfaces, Hard Furniture, Sanitary Equipment, External Surfaces Of Devices, Medical Products, For Infections Of Bacterial (Including Tuberculosis), Viral And Fungal Etiology During Preventive, Current And Final Disinfection In Medical Facilities; - Carrying Out General Cleaning. The Shelf Life Of The Product Is At Least 6 Years, Working Solutions - 20 Days. The Product Must Contain At Least 300 Tablets In One Jar., The Disinfectant Should Be A Ready-To-Use Skin Antiseptic In The Form Of A Clear, Colorless Liquid With A Characteristic Alcoholic Odor. The Product Must Contain Isopropyl Alcohol 65.0 ± 5.0%, Glycerin 0.4 ± 0.2%, Allontoin As Active Ingredients (Ai), As Well As Functional Additives And Water. The Ph Of A 1% Aqueous Solution Of The Product Should Be In The Range Of 6.5 ± 1.0%. The Product Must Have Bactericidal, Virucidal, Tuberculocidal (Tested Against M. Terrae), Fungicidal Activity, And Also Be Active Against Particularly Dangerous Infections (Plague, Cholera, Tularemia). The Product Should Be Intended For: Hygienic Treatment Of The Hands Of Staff, Patients And Visitors Of Medical And Preventive And Other Institutions And Organizations; Surgical Treatment Of The Hands Of Surgeons Of All Specialties; Skin Treatment Before Inserting Catheters And Puncture Of Joints; Treatment Of Donor Elbows At Blood Transfusion Stations; Treating The Skin Of The Surgical Field Of Patients, The Injection Field (For Intradermal, Subcutaneous, Intramuscular, Intravenous And Other Injections) In Health Care Facilities And Organizations; Disinfection Of Gloves Worn By Personnel; Disinfection Of Medical Products. Shelf Life: At Least 3 Years. Euro Bottle With A Volume Of At Least 1 Liter., Napkins In A Roll Made Of Spinlace Size 30*140Cm Density 40 G/M2 Non-Sterile No. 200 Pcs, The Disinfectant (Concentrate) Must Contain Stabilized Hydrogen Peroxide 20%, Glycolic Acid In The Range Of 0.7-1.7%, As Well As A Surfactant, Complexing Agent, Hydrogen Peroxide Stabilizer, Corrosion Inhibitor, And Water. The Product Should Not Contain Alcohols, Aldehydes, Naa, Has, Guanidine, Amines, Chlorine, Phenol, Aromatic Fragrances. The Ph Should Be 1.5 - 5.5%. The Product Must Have Bactericidal, Virucidal, Tuberculocidal (Against The Pathogen M. Terrae), Fungicidal, Sterilizing (Sporicidal) Activity, As Well As Activity Against Especially Dangerous Infections (Plague, Cholera, Tulerymia, Brucellosis, Anthrax). The Product Must Be Approved For Use For: Disinfection Of Incubators, Anesthesia-Respiratory Equipment, Anesthesia Equipment, Breathing Circuits, Bags, Ultrasound Sensors, Resuscitation And Changing Tables; For Disinfection And Pso (Including Those Combined In One Process) Of Medical Devices (Including Endoscopes); Sterilization Of Medical Devices (Including Endoscopes); Tld Endoscopes; Disinfection Of Various Medical Equipment. The Time For Carrying Out Hld Endoscopes At A Temperature Of At Least 18 °C Is No More Than 5 Minutes, Sterilization Of Medical Devices Is No More Than 10 Minutes. The Time For Performing Tld Endoscopes At A Temperature Of At Least 50 °C Is 3 Minutes. In The Working Solution Of The Product Used For Hld Endoscopes And Sterilization Of Medical Devices, The Content Of Hydrogen Peroxide Should Be 6%. Shelf Life Is At Least 2 Years, Working Solutions Are At Least 18 Days. The Product Must Be Accompanied By Indicator Strips For Iec Express Control (Up To 100 Liters Of Concentrate 1 Package, Then For Every 100 Liters Of Concentrate 1 Package). Euro Bottle With A Volume Of At Least 1 Liter