Disinfectant (Liquid Concentrate With A Cleaning Effect), With A Volume Of At Least 5 Liters. The Product Must Contain A Concentrate Containing Enzymes (Protease, Amylase, Pectinase, Lipase, Mannanase), As Well As A Number Of Functional Additives (Nonionic Surfactants, Enzyme Stabilizers, Detergents, Ph Stabilizers, Dye) And Water. The Ph Of The Product Should Be In The Range Of 6.3-8.5. The Product Should Not Contain Any Other Additional Ingredients (Alcohols, Aldehydes, Hydrogen Peroxide, Qas, Phenol Derivatives, Guanidine, Alkylamines). The Product Must Have Fivefold Proteolytic Activity And High Detergent Properties With Low Foaming. The Product Must Not Be Corrosive So As Not To Damage Products Made Of Metals (Stainless And Carbon Steel), As Well As Plastics And Rubber. The Product Must Be Approved For Use For Pre-Sterilization Cleaning Of Medical Devices Made Of Various Materials, Rigid And Flexible Endoscopes And Instruments For Them, Final Cleaning Of Endoscopes Before Hld And Sterilization. There Is A Valid Certificate, Certificate Or Passport Of State Registration Of The Product, Instructions For Use Attached To It And It Is Approved For Use In The Territories Of The Republic Of Kazakhstan. Container Requirements: The Lid Must Be Tightly Closed To Prevent Evaporation And Spilling Of The Contents. The Container Must Not Have Any Damage That Could Cause Leakage Or Other Problems. Container Material: Plastic Matte Container (To Prevent Direct Exposure To Sunlight). Storing The Product In The Manufacturers Container (Without Transfusion). The Package Must Have A Label Indicating The Name, Concentration, Date Of Preparation, And Expiration Date. Gbmp (Medical University Clinic), Dry Wipes Dezon For Dispenser, Size 140X210 Mm. A Replaceable Block Of Dezon Napkins Is Used Separately Or In The Dezon Dispensary System. Size 140 X 210 Mm. 300 Pcs Per Roll. Designed For Impregnation With Cleaning, Disinfectant Or Plain Water. Also, The Wipes Can Be Used Without Impregnation If Dry Cleaning Is Needed. Made From High-Quality Materials, Leaving No Lint On Surfaces, Soft, Elastic And Pleasant To The Touch, Optimal Level Of Tear Strength, Good Moisture Absorption, Environmentally Friendly. Each Roll Has A Perforation Line. Gbmp (Medical University Clinic), Antiseptic (Skin Antiseptic) 1 Liter. The Product Is A Ready-To-Use Skin Antiseptic Of Various Colors And Is Available In The Form Of A Clear, Colorless Liquid With A Characteristic Alcoholic Odor. Contains: Isopropyl Alcohol 50%, Propyl Alcohol 20%, Alkyldimethylbenzylammonium Chloride 0.10% As Active Ingredients (Ai), As Well As Functional Additives And Water; The Colored Modification Additionally Includes Food Coloring. Volume: 1 L. There Is A Valid Certificate, Certificate Or Passport Of State Registration Of The Product, Instructions For Use Attached To It And It Is Approved For Use In The Territories Of The Republic Of Kazakhstan. Container Requirements: The Lid Must Be Tightly Closed To Prevent Evaporation And Spilling Of The Contents. The Container Must Not Have Any Damage That Could Cause Leakage Or Other Problems. Container Material: Plastic Matte Container (To Prevent Direct Exposure To Sunlight). Storing The Product In The Manufacturers Container (Without Transfusion). The Package Must Have A Label Indicating The Name, Concentration, Date Of Preparation, And Expiration Date. Gbmp (Medical University Clinic), Antiseptic (Skin Antiseptic) 5 Liters. The Product Is A Ready-To-Use Skin Antiseptic Of Various Colors And Is Available In The Form Of A Clear, Colorless Liquid With A Characteristic Alcoholic Odor. Contains: Isopropyl Alcohol 50%, Propyl Alcohol 20%, Alkyldimethylbenzylammonium Chloride 0.10% As Active Ingredients (Ai), As Well As Functional Additives And Water; The Colored Modification Additionally Includes Food Coloring. Volume: 5 L There Is A Valid Certificate, Certificate Or Passport Of State Registration Of The Product, Instructions For Use Attached To It And Approved For Use In The Territories Of The Republic Of Kazakhstan. Container Requirements: The Lid Must Be Tightly Closed To Prevent Evaporation And Spilling Of The Contents. The Container Must Not Have Any Damage That Could Cause Leakage Or Other Problems. Container Material: Plastic Matte Container (To Prevent Direct Exposure To Sunlight). Storing The Product In The Manufacturers Container (Without Transfusion). The Package Must Have A Label Indicating The Name, Concentration, Date Of Preparation, And Expiration Date. Gbmp (Medical University Clinic)., Disinfectant (Ready Solution), Volume Of At Least 5 Liters. The Disinfectant (Ready Solution) Must Contain Orthophthalaldehyde As An Active Ingredient In The Range Of 0.6-0.65%, As Well As Surfactants, Auxiliary Components And Water. The Ph Of The Product Should Be In The Range Of 7.0-8.5%. The Product Must Be Well Compatible With Various Materials Of Medical Devices, Not Destroy The Surface Being Treated, Not Cause Corrosion Of Metals, Including Aluminum, Carbon Steel, Chromium And Nickel, Not Destroy Adhesive Compounds And Elastomers, And Not Cause Clouding Of Optics. The Product Must Be Approved For Use For The Disinfection Of Medical Devices Made Of Various Materials, Rigid And Flexible Endoscopes, And Instruments For Them, Manually, Mechanized And Automated; Tld Of Rigid And Flexible Endoscopes In Manual, Mechanized And Automated Ways (Automatic Installation For Washing And Tld Of Endoscopes). Shelf Life Is At Least 3 Years In Unopened Manufacturers Packaging, In An Opened Canister For At Least 80 Days. Repeated Use Of The Product For At Least 30 Days. For Express Control Of Mdc, The Product Must Have Indicator Strips. There Is A Valid Certificate, Certificate Or Passport Of State Registration Of The Product, Instructions For Use Attached To It And It Is Approved For Use In The Territories Of The Republic Of Kazakhstan. Container Requirements: The Lid Must Be Tightly Closed To Prevent Evaporation And Spilling Of The Contents. The Container Must Not Have Any Damage That Could Cause Leakage Or Other Problems. Container Material: Plastic Matte Container (To Prevent Direct Exposure To Sunlight). Storing The Product In The Manufacturers Container (Without Transfusion). The Package Must Have A Label Indicating The Name, Concentration, Date Of Preparation, And Expiration Date. (Medical University Clinic), Disinfectant With A Volume Of 5 Liters. With 1 L. Concentrate, 100 Liters Of Ready-Made Working Solution Are Prepared. Belongs To Class 4 Of Low-Hazard Substances When Applied To The Skin. Solutions Of The Product Do Not Change The Quality Of The Objects Being Treated (Including Various Brands Of Plexiglass), Do Not Form A Film On Them, Do Not Cause Corrosion Of Stainless Metal, And Do Not Discolor Fabrics. Universal Action (Disinfection, Hld, Pso, Sterilization). They Have Cleaning And Deodorizing Properties. The Working Solution Life Is 14 Days. The Shelf Life Of The Product Is 5 Years. Ingredients: Qac (Alkyldimethylbenzylammonium Chloride) – 2.5%, Glutaraldehyde -2.5%, Surfactant, Flavoring. Ingredients: Qac (Alkyldimethylbenzylammonium Chloride) – 2.5%, Glutaraldehyde -2.5%, Surfactant, Flavoring, Distilled Water. Volume: 5 L. There Is A Valid Certificate, Certificate Or Passport Of State Registration Of The Product, Instructions For Use Attached To It And It Is Approved For Use In The Territories Of The Republic Of Kazakhstan. Container Requirements: The Lid Must Be Tightly Closed To Prevent Evaporation And Spilling Of The Contents. The Container Must Not Have Any Damage That Could Cause Leakage Or Other Problems. Container Material: Plastic Matte Container (To Prevent Direct Exposure To Sunlight). Storing The Product In The Manufacturers Container (Without Transfusion). The Package Must Have A Label Indicating The Name, Concentration, Date Of Preparation, And Expiration Date. Gbmp (Medical University Clinic), Disinfectant (Liquid Concentrate With A Cleaning Effect), With A Volume Of At Least 5 Liters. The Product Must Contain A Concentrate Containing Enzymes (Protease, Amylase, Pectinase, Lipase, Mannanase), As Well As A Number Of Functional Additives (Nonionic Surfactants, Enzyme Stabilizers, Detergents, Ph Stabilizers, Dye) And Water. The Ph Of The Product Should Be In The Range Of 6.3-8.5. The Product Should Not Contain Any Other Additional Ingredients (Alcohols, Aldehydes, Hydrogen Peroxide, Qas, Phenol Derivatives, Guanidine, Alkylamines). The Product Must Have Fivefold Proteolytic Activity And High Detergent Properties With Low Foaming. The Product Must Not Be Corrosive So As Not To Damage Products Made Of Metals (Stainless And Carbon Steel), As Well As Plastics And Rubber. The Product Must Be Approved For Use For Pre-Sterilization Cleaning Of Medical Devices Made Of Various Materials, Rigid And Flexible Endoscopes And Instruments For Them, Final Cleaning Of Endoscopes Before Hld And Sterilization. The Product Must Be Applied Manually And, Without Fail, Mechanized In Ultrasonic Installations And Automated In A Washing-Disinfecting Machine (Wdm) At Room Temperature. There Is A Valid Certificate, Certificate Or Passport Of State Registration Of The Product, Instructions For Use Attached To It And It Is Approved For Use In The Territories Of The Republic Of Kazakhstan. Container Requirements: The Lid Must Be Tightly Closed To Prevent Evaporation And Spilling Of The Contents. The Container Must Not Have Any Damage That Could Cause Leakage Or Other Problems. Container Material: Plastic Matte Container (To Prevent Direct Exposure To Sunlight). Storing The Product In The Manufacturers Container (Without Transfusion). The Package Must Have A Label Indicating The Name, Concentration, Date Of Preparation, And Expiration Date. Medical University Clinic, Disinfectant (Ready Solution), Volume Of At Least 5 Liters. The Disinfectant (Ready Solution) Must Contain Orthophthalaldehyde As An Active Ingredient In The Range Of 0.6-0.65%, As Well As Surfactants, Auxiliary Components And Water. The Product Should Not Contain Other Active Ingredients. The Ph Of The Product Should Be In The Range Of 7.0-8.5%. The Product Must Have Antimicrobial Activity Against Various Gram-Negative And Gram-Positive Bacteria, Mycobacterium Tuberculosis, Viruses, And Sporicidal Activity. The Product Must Be Well Compatible With Various Materials Of Medical Devices, Not Destroy The Surface Being Treated, Not Cause Corrosion Of Metals, Including Aluminum, Carbon Steel, Chromium And Nickel, Not Destroy Adhesive Compounds And Elastomers, And Not Cause Clouding Of Optics. The Product Must Be Approved For Use For The Disinfection Of Medical Devices Made Of Various Materials, Rigid And Flexible Endoscopes, And Instruments For Them, Manually, Mechanized And Automated; Tlds Of Rigid And Flexible Endoscopes In Manual, Mechanized And Automated Ways. Shelf Life Is At Least 3 Years In Unopened Manufacturers Packaging, In An Opened Canister For At Least 80 Days. Repeated Use Of The Product For At Least 30 Days. There Is A Valid Certificate, Certificate Or Passport Of State Registration Of The Product, Instructions For Use Attached To It And It Is Approved For Use In The Territories Of The Republic Of Kazakhstan. Container Requirements: The Lid Must Be Tightly Closed To Prevent Evaporation And Spilling Of The Contents. The Container Must Not Have Any Damage That Could Cause Leakage Or Other Problems. Container Material: Plastic Matte Container (To Prevent Direct Exposure To Sunlight). Storing The Product In The Manufacturers Container (Without Transfusion). The Package Must Have A Label Indicating The Name, Concentration, Date Of Preparation, And Expiration Date. Gbmp (Medical University Clinic), Disinfectant, Tableted, With A Volume Of At Least 90 Pieces (Tablets) In 1 Package. The Disinfectant Is A Tablet Weighing 3.4 Grams And Granules With A Slight Odor Of Chlorine, Fragrances Containing The Sodium Salt Of Dichloroisocyanuric Acid As An Active Ingredient, As Well As Surfactants And Special Additives. Active Chlorine Content In The Product 44.2 ± 4.0%, Surfactant Content - 1.5 ± 0.5%. When 1 Tablet Is Dissolved In Water, 0.75 ± 0.07 Or 1.5 ± 0.15 Grams Of Active Chlorine Are Released (For Tablets Weighing 1.7 And 3.4 Grams Respectively). The Product Is Available In Plastic Packaging Of 90 Pieces (Tablets). The Shelf Life Of The Product (Tablets And Granules) In Unopened Manufacturer’S Packaging Is 7 Years. The Shelf Life Of Working Solutions Of The Product Is 22 Days. The Disinfectant Has A Full Spectrum Of Antimicrobial Activity: Bactericidal [Incl. Tuberculocidal, Pathogens Of Nosocomial Infections, Acute Infectious Diseases (Plague, Cholera, Tularemia, Anthrax), Virucidal (Including Pathogens Of Hiv Infection, Hepatitis, Influenza H1n1, H5n1, Polio), Fungicidal (Including The Genera Candida, Trichophyton, Aspergillus), Sporicidal, Ovocidal (Pathogens Of Parasitic Diseases). There Is A Valid Certificate, Certificate Or Passport Of State Registration Of The Product, With Instructions For Use Attached To It. Gbmp (Medical University Clinic)., Dispenser For Dry Wipes Dezon 3.8 Liters. The Dispenser Is Designed For Dry Wipes (Replaceable Blocks) Dezon Made Of White Non-Woven Material, Divided By A Perforated Line Into Separate Wipes. The Dispenser Can Be In The Form Of A Jar Made Of Dense Polymer In Accordance With Gost R 51760-2001 With Double Clamping Lids, The Inner Lid Has A Functional Slot In The Center, Or Buckets With A Handle And A Lid With A Dosing Valve. Gbmp (Medical University Clinic)
