Tenders Are Invited For Purchase Of Goods

Disinfectant, Skin Antiseptic, Ready-To-Use Solution. The Product Is A Ready-To-Use Skin Antiseptic In The Form Of A Colorless, Transparent Liquid With A Characteristic Odor. Contains As Active Ingredients Propanol 1 No More Than 50%, Propanol 2 No More Than 10%, Alkyl-Benzyl-Dimethylammonium Chloride (Not Less Than 0.7% And Not More Than 0.8%), Polyethylene Glycol Ether Of Fatty Alcohol (Not Less Than 0.05% And Not More Than 00.55%) Sodium Ethylenediaminetetraacetic Acid (Not Less Than 0.03 % And Not More Than 0.035%), Trisodium Salt Of Nitrilotriacetic Acid (Not Less Than 0.02% And Not More Than 0.025%), Tetrapotassium Diphosphate Salt (Not Less Than 0.02% And Not More Than 0.025%), Cocamidopropylamine Oxide (Not Less Than 0.02% And Not More Than 0.025%), Hexylsinnamal (Not Less Than 0.01% And Not More 0.015%), Linalool (Not Less Than 0.01% And Not More Than 0.015%), Butylphenylmethylpropional (Not Less Than 0.01% And Not More Than 0.015%) The Shelf Life Of The Product Is 5 Years In Unopened Sealed Packaging From The Manufacturer. The Product Is Intended As A Skin Antiseptic: - For Hygienic Treatment Of The Hands Of Medical Personnel In Medical And Preventive Institutions; - For Treating The Hands Of Surgeons, Operating Nurses And Other Persons Involved In Operations In Medical Institutions; - Elbow Bends Of Donors, Skin Of Surgical And Injection Fields. To Confirm The Declared Technical Properties Of The Product, The Potential Supplier Attaches To The Application Electronic Copies Of Documents: Methodological Instructions In The Kazakh And Russian Languages, With The Mandatory Content Of Information On The Quantitative And Qualitative Composition Of The Product, Indicating The Active Substances And Their Concentration, As Well As Information Regarding Methods Of Quality Control Of The Product; Certificate Of State Registration Of Goods On The Territory Of The Customs Union When Submitting An Application, The Potential Supplier Must Attach St-Kz, Sgr, Instructions For Use, Dry Wipes No. 200. The Roll Of Wipes Must Be Supplied In An Individual Sealed Plastic Packaging Containing A Roll Of Dry Wipes With A Self-Adhesive Form. This Form Must Contain The Following Fields: Name Of The Product, Concentration Of The Solution, Disinfection Time, Batch Number, Expiration Date, Name Of The Employee Who Poured The Solution. There Are No Less Than 119 But No More Than 200 High-Strength Perforated Napkins Per Roll. The Main Size Of One Napkin Per Roll Is 15 ± 0.5 Cm × 30 ± 0.5 Cm (Folded). When Removed From The Dispenser, Each Napkin Automatically Unfolds Into A Candy-Shaped Form, Providing Full Expansion To A Size Of 30 ± 0.5 Cm × 30 ± 0.5 Cm (Unfolded). The Perforation Line Separating One Napkin From Another Must Be Clear To Ensure Their Economical Consumption. The Material From Which Napkins Are Made Must Contain At Least 40% Viscose And No More Than 60% Polyester. Material Density Is Not Less Than 60 G/M2. The Soaking Time Of Napkins With Liquid Detergent Or Disinfectant Should Be No More Than 1 Minute. The Volume Of Product Required For Uniform Impregnation Of Napkins Is 0.5 Liters. Also, Napkins Can Be Used Without Impregnation Instead Of Rags And Rags If Dry Cleaning Is Needed. The Treatment Area With One Napkin Is At Least 2 Square Meters. The Shelf Life Of The Replacement Unit In Individual Sealed Plastic Packaging Is Unlimited. Made In Kazakhstan. When Submitting An Application, The Potential Supplier Must Attach A Registration Certificate (Ra), St-Kz, Sgr, Instructions For Use, Medical Soap. The Product Is A Ready-To-Use Substance With A Gel-Like Consistency. It Contains Lactic Acid, Propylene Glycol, Cocamide Dea, Sodium Laureth Sulfate, Cocomidopropyl Betaine, Glycerin, Etc. Ph Of The Product Is 5.5 ± 1.0. The Product Should Not Contain Polyhexamethylene Guanidine, Polyhexamethylene Biguanidine, Triclosan, Hour, Glutaraldehyde, Tetranyl U, Fragrances, Extracts And Herbal Decoctions. The Product Has Antibacterial Activity Against Gram-Negative And Gram-Positive (Except For Mycobacterium Tuberculosis) Bacteria, Fungicidal Activity Against Yeast-Like Fungi, And Virucidal Activity. In Terms Of Acute Toxicity Parameters, According To Gost 12.1.007-76, When Administered Into The Stomach And Applied To The Skin, It Belongs To The 4Th Class Of Low-Hazard Compounds. Local Irritant, Skin-Resorptive And Sensitizing Properties Are Not Expressed Upon Repeated Exposure. Application Of The Product To Scarified Skin Does Not Complicate Artificially Inflicted Wounds. The Product Is Intended: For Washing The Hands Of Surgeons And Operating Medical Personnel Before Treatment With An Antiseptic; Hygienic Treatment Of The Patient’S Skin Before Surgery; Hygienic Treatment Of Hands Before And After Medical Procedures By Employees Of Health Care Facilities, Maternity Hospitals, Preschool And School Institutions, Social Security Institutions; Hygienic Treatment Of Hands And Sanitary Treatment Of Skin In Institutions Of Various Profiles. The Shelf Life Of The Product Is 3 Years From The Date Of Manufacture When Stored In Unopened Packaging Of The Manufacturer. Labeling Data Contains In The State And Russian (Two!) Languages: Name Of The Manufacturer, Name And Purpose Of The Product, Method Of Application, Net Weight, Month And Year Of Production, Precautions And Protective Equipment, Designation Of The Organizations Standard. The Supplier Attaches To The Application Certificate Of State Registration Of Goods In The Territory Of The Customs Union.