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Campylobagar Is A Completely Ready-To-Use Nutrient Medium Intended For The Isolation, Selection And Cultivation Of Bacteria Of The Genus Campylobacter. Packaged In Bottles Of No More Than 0.5 Kg. A Label Is Placed On The Bottles, Which Indicates: The Manufacturing Organization, Its Address And Trademark, The Full Name Of The Drug, Its Composition, Series (Batch) Number, Production Date, Expiration Date (Month, Year), Weight Of The Drug, Storage Conditions. Each Bottle Is Accompanied By Instructions For Use (Preparation) With A Notarized Translation Into The State And Russian Languages. Packaged In Boxes (Boxes) With Sealing Filling. The Shelf Life Is At Least 80% From The Date Of Manufacture At The Time Of Delivery (With A Shelf Life Of Twelve To Twenty-Four Months) And At Least 60% From The Date Of Manufacture At The Time Of Delivery (With A Shelf Life Of More Than Twenty-Four Months). Providing Documents Confirming The Quality Of The Drug. Additional Doses For Incoming Control From Each Batch In The Amount Of One Packaging Unit., Negative Brucellosis Serum For Control In The Diagnosis Of Brucellosis In Animals. Lyophilized Homogeneous Porous Mass, Intended To Control The Agglutination Reaction, Complement Fixation Reaction, Long-Term Complement Fixation Reaction, Packaged In Ampoules/Vials With A Volume Of At Least 2.0 Cm³, But Not More Than 5.0 Cm³, Indicating The Series And Date Of Manufacture, Expiration Date On Each Ampoule/Vial And On The Box In The Form Of An Imprint. The Drug Should Be Packaged In Cardboard Boxes Of No More Than 10 Ampoules/Bottles. At The Time Of Delivery Of The Goods, The Supplier Must Provide The Following: 1. Providing A Copy Of The Instructions For Use In The State And Russian Languages. 2. Each Box Must Indicate The Series, Expiration Date, Date Of Manufacture, Cm3 Volume, Name And Trademark Of The Manufacturer’S Organization, Its Address, Full Name Of The Kit, List Of Components Included In The Kit, Storage Conditions. 3. A Copy Of Documents Of Production Compliance With International Standards; 4. Shelf Life Is At Least 80% From The Date Of Manufacture At The Time Of Delivery (With A Shelf Life Of Twelve To Twenty-Four Months) And At Least 60% From The Date Of Manufacture At The Time Of Delivery (With A Shelf Life Of More Than Twenty-Four Months). 5. The Drug Must Be Packaged In Cardboard Boxes. 6. Each Kit Must Contain Official Instructions From The Manufacturer With A Notarized Translation Into The State And Russian Languages. 7. The Box Must Contain The Inscription “For Veterinary Use.” 8. Boxes Must Be Placed In Boxes With Thermal Insulation And Sealing Filling. 9. Providing Evidence Of Compliance With Temperature Conditions During Transportation. 10. Additional Doses For Carrying Out Incoming Control From Each Batch In The Amount Of One Packaging Unit. 11.Providing A Document Confirming The Quality Of The Drug With A Notarized Translation Into The State And Russian Languages., Hisss Medium With Dulcite. Must Be Packaged In Bottles Of No More Than 0.5 Kg. A Label Is Attached To The Container Indicating: The Manufacturers Organization, Its Address And Trademark, The Full Name Of The Drug, Its Composition, Series (Batch) Number, Production Date, Expiration Date (Month, Year), Weight Of The Drug, Storage Conditions. Availability Of Instructions For Use (Preparation) From The Manufacturer With A Notarized Translation Into State And Russian Languages. Shelf Life Is At Least 12 Months And At Least 80% From The Date Of Manufacture To The Time Of Delivery. Providing A Document Confirming The Quality Of The Product With A Notarized Translation Into The State And Russian Languages., Anthrax Bacterial Antigen. The Drug Is Intended To Control The Activity And Specificity Of Anthrax Precipitating Serum In The Diffuse Precipitation Reaction. Sterile, Clear Liquid. Available In Ampoules Or Bottles Of No More Than 1 Ml. At The Time Of Delivery Of The Goods, The Supplier Must Provide The Following: 1. Providing A Copy Of The Instructions For Use In The State And Russian Languages. 2. Each Box Must Indicate The Series, Expiration Date, Date Of Manufacture, Cm3 Volume, Name And Trademark Of The Manufacturer’S Organization, Its Address, Full Name Of The Kit, List Of Components Included In The Kit, Storage Conditions. 3. A Copy Of Documents Of Production Compliance With International Standards; 4. Shelf Life Is At Least 80% From The Date Of Manufacture At The Time Of Delivery (With A Shelf Life Of Twelve To Twenty-Four Months) And At Least 60% From The Date Of Manufacture At The Time Of Delivery (With A Shelf Life Of More Than Twenty-Four Months). 5. The Drug Must Be Packaged In Cardboard Boxes. 6. Each Kit Must Contain Official Instructions From The Manufacturer With A Notarized Translation Into The State And Russian Languages. 7. The Box Must Contain The Inscription “For Veterinary Use.” 8. Boxes Must Be Placed In Boxes With Thermal Insulation And Sealing Filling. 9. Providing Evidence Of Compliance With Temperature Conditions During Transportation. 10. Additional Doses For Carrying Out Incoming Control From Each Batch In The Amount Of One Packaging Unit. 11.Providing A Document Confirming The Quality Of The Drug With A Notarized Translation Into The State And Russian Languages., Hiss Medium With Raffinose. Must Be Packaged In Bottles Of No More Than 0.5 Kg. A Label Is Placed On The Container Indicating: The Manufacturers Organization, Its Address And Trademark, The Full Name Of The Drug, Its Composition, Series (Batch) Number, Production Date, Expiration Date (Month, Year), Weight Of The Drug, Storage Conditions. Availability Of Instructions For Use (Preparation) From The Manufacturer With A Notarized Translation Into The State And Russian Languages. Shelf Life Is At Least 12 Months And At Least 80% From The Date Of Manufacture To The Time Of Delivery. Providing A Document Confirming The Quality Of The Goods With A Notarized Translation Into The State And Russian Languages., Fluorescent Immersion Oil, Transparent Light Yellow Liquid Without Bubbles And Foreign Inclusions With A Slight Specific Odor, Packaged In Bottles, No More Than 0.02 Kg. Gost 13739-78. A Label Is Placed On The Bottles Indicating: The Manufacturers Organization, Its Address And Trademark, The Full Name Of The Drug, Series (Batch) Number, Production Date, Expiration Date (Month, Year), Weight Of The Drug, Storage Conditions. Packed In Boxes With Thermal Insulation And Sealing Filling. Shelf Life Is At Least 80% From The Date Of Manufacture At The Time Of Delivery (With A Shelf Life Of Twelve To Twenty-Four Months) And At Least 60% From The Date Of Manufacture At The Time Of Delivery (With A Shelf Life Of More Than Twenty-Four Months). Providing A Document Confirming The Quality Of The Goods With A Notarized Translation Into The State And Russian Languages., Vaseline Medical Oil Gost 3164-78. Packaged In Bottles, No More Than 0.1 Kg. A Label Is Placed On The Bottles Indicating: The Manufacturing Organization, Its Address And Trademark, The Full Name Of The Drug, Series (Batch) Number, Production Date, Expiration Date (Month, Year), Weight Of The Drug, Storage Conditions. Shelf Life Is At Least 80% From The Date Of Manufacture To The Time Of Delivery. Providing A Document Confirming The Quality Of The Goods With A Notarized Translation Into The State And Russian Languages., Benzylpenicillin. White Fine Powder In Bottles No More Than 1,000,000 Units. The Bottles Are Packed In Boxes, No More Than 40 Pieces Per Box. Indicating On The Box And Bottles The Name And Trademark Of The Manufacturer, Its Address, The Full Name Of The Drug, Date Of Manufacture, Batch (Batch) Number, Expiration Date, Storage Conditions. The Shelf Life Is At Least 80% From The Date Of Manufacture At The Time Of Delivery (With A Shelf Life Of Twelve To Twenty-Four Months) And At Least 60% From The Date Of Manufacture At The Time Of Delivery (With A Shelf Life Of More Than Twenty-Four Months). Providing A Document Confirming The Quality Of The Goods With A Notarized Translation Into The State And Russian Languages., Ready-To-Use Romanovsky-Giemsa Paint In Bottles (Made Of Darkened Material) No More Than 1 Liter. A Label Is Placed On The Bottles, Which Indicates: The Manufacturing Organization, Its Address And Trademark, The Full Name Of The Drug, Its Composition, Series (Batch) Number, Production Date, Expiration Date (Month, Year), Weight Of The Drug, Storage Conditions. Shelf Life Is At Least 80% From The Date Of Manufacture At The Time Of Delivery (With A Shelf Life Of Twelve To Twenty-Four Months) And At Least 60% From The Date Of Manufacture At The Time Of Delivery (With A Shelf Life Of More Than Twenty-Four Months). Each Bottle Is Accompanied By Instructions For Use (Preparation) With A Notarized Translation Into The State And Russian Languages. Packaged In Boxes With Thermal Insulation And Sealing Filling. Providing A Document Confirming The Quality Of The Goods With A Notarized Translation Into The State And Russian Languages., .Positive Brucellosis Serum For Control In The Diagnosis Of Brucellosis In Animals. According To Technical Specification, The Set Of Reagents Is Intended For Use As A Growth-Stimulating Component Of Bacteriological Nutrient Media Used For The Cultivation Of Microorganisms. It Is A Native Serum Obtained From The Blood Of Donor Horses. Sterile. Packaged In Ampoules/Bottles With A Volume Of No More Than 400 Ml. The Box And Ampoule Must Indicate The Name And Trademark Of The Manufacturing Organization, Its Address, The Full Name Of The Drug, Date Of Manufacture, Batch (Batch) Number, Expiration Date, Weight Of The Drug, Storage Conditions. The Shelf Life Is At Least 80% From The Date Of Manufacture At The Time Of Delivery (With A Shelf Life Of Twelve To Twenty-Four Months) And At Least 60% From The Date Of Manufacture At The Time Of Delivery (With A Shelf Life Of More Than Twenty-Four Months). Providing Documents Confirming The Quality Of The Drug. Additional Doses For Incoming Control From Each Batch In The Amount Of One Packaging Unit. Provision Of A Document Confirming The Quality Of The Product With A Notarized Translation Into The State And Russian Languages., Erythritol Agar. For The Cultivation Of Brucella. Dry, Light Yellow In Color, Powdery, In Plastic Bottles No More Than 0.25 Kg. A Label Is Placed On The Bottles, Which Indicates: The Manufacturing Organization, Its Address And Trademark, The Full Name Of The Drug, Its Composition, Series (Batch) Number, Production Date, Expiration Date (Month, Year), Weight Of The Drug, Storage Conditions. Each Bottle Is Accompanied By Instructions For Use (Preparation) With A Notarized Translation Into The State And Russian Languages. Packed In Boxes With Thermal Insulation And Sealing Filling. Shelf Life Is At Least 80% From The Date Of Manufacture At The Time Of Delivery (With A Shelf Life Of Twelve To Twenty-Four Months) And At Least 60% From The Date Of Manufacture At The Time Of Delivery (With A Shelf Life Of More Than Twenty-Four Months). Providing Documents Confirming The Quality Of The Drug., Ethyl Alcohol. Ethyl Alcohol, Packaged In Plastic Containers With A Volume Of No More Than 5 Liters. Transparent Liquid With A Characteristic Odor. Gost 5962-2013, Not Less Than 96.3 Degrees. Indicating On The Bottles The Name And Trademark Of The Manufacturers Organization, Its Address, The Full Name Of The Drug, Dates Of Manufacture, Series (Batch) Number, Expiration Date, Weight Of The Drug, Storage Conditions. The Shelf Life Is At Least 80% From The Date Of Manufacture At The Time Of Delivery (With A Shelf Life Of Twelve Twenty-Four Months) And At Least 60% From The Date Of Manufacture At The Time Of Delivery (With A Shelf Life Of More Than Twenty-Four Months). Providing A Document Confirming The Quality Of The Drug With A Notarized Translation Into The State And Russian Languages.
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