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Kit For Serological Diagnosis Of Trypanosomosis Of Horses And Camels In Rsk. According To The Technical Specification, Kit For Diagnosis Of Infectious Anemia Of Horses In Response To Diffuse Precipitation. According To The Technical Specification, Kit For Immunodiffusion Reaction To Antibodies To Leukemia In Agricultural Animals. According To The Technical Specification, Set Of Immunoenzymatic Analysis For The Diagnosis Of Paratuberculosis. According To The Technical Specification, Bacterial Anthrax Antigen. The Drug Is Intended For Monitoring The Activity And Specificity Of Anthrax Precipitating Serum In The Reaction Of Diffuse Precipitation. Sterile, Transparent Liquid. Available In Ampoules Or Vials Of No More Than 1 Ml. At The Time Of Delivery Of The Goods, The Supplier Must Provide The Following: 1. Each Box And Ampoule (Flacon) Must Have The Series, Control, Date Of Manufacture, Expiration Date, Volume Cm3, Name And Trademark Of The Manufacturers Organization, Its Address, Full Name Of The Set, List Components Included In The Set, Storage Conditions. 2. Copy Of Documents Of Production Compliance With International Standards. 3. The Shelf Life Is Not Less Than 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). 4. The Drug Must Be Packed In Cardboard Boxes. 5. Each Box Must Contain Instructions Or Instructions For Their Use In The State And Russian Languages. 6. The Inscription For Veterinary Use Must Be On The Box. 7.. Providing Evidence Of Compliance With The Temperature Regime During Transportation. 8. Will Provide Additional Samples For Input Control. 9. Submission Of A Document Confirming The Quality Of The Drug With An Official Translation Into The State And Russian Languages., Polymerase Chain Reaction Is A Test Substance For Determining The Causative Agent Of Brucellosis. According To The Technical Description, Test System For The Identification Of The Causative Agent Of Anthrax By The Polymerase Chain Reaction Method In Real Time. According To The Technical Specification, Fluorescent Immersion Oil, Transparent Light Yellow Liquid Without Bubbles And Foreign Inclusions With A Weak Specific Smell, Packaged In Bottles, No More Than 0.02 Kg. Gost 13739-78. A Label Is Affixed To The Vials Indicating: The Manufacturers Organization, Its Address And Trademark, The Full Name Of The Drug, The Batch Number, The Date Of Manufacture, The Expiration Date (Months, Hours), The Weight Of The Drug, And Storage Conditions. They Are Packed In Boxes With Thermal Insulation And Sealing Filling. The Shelf Life Is Not Less Than 80% From The Date Of Manufacture At The Time Of Delivery (With A Shelf Life Of Twelve To Twenty Four Months) And Not Less Than 60% From The Date Of Manufacture At The Time Of Delivery (With A Shelf Life Of More Than Twenty Four Months). Provision Of A Document Confirming The Quality Of The Drug., Ready-To-Use Romanovsky-Gymza Paint In Bottles (Made Of Tinted Material) Of No More Than 1 Liter. A Label Is Affixed To The Vials, Which Indicates: The Manufacturers Organization, Its Address And Trademark, The Full Name Of The Drug, Its Composition, Series (Batch) Number, Date Of Manufacture, Expiration Date (Month, Hour), Weight Of The Drug, Storage Conditions. The Shelf Life Is Not Less Than 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 Months). Instructions For Use (Preparation) Are Attached To Each Bottle In Russian And The State Language. They Are Packed In Boxes With Thermal Insulation And Sealing Filling. Provision Of Documents Confirming The Quality Of The Drug., Benzylpenicillin. White Fine Powder In Vials Of No More Than 1,000,000 Units. Vials Are Packed In Boxes, No More Than 40 Pieces In A Box. With An Indication On The Box And Bottles Of The Name And Trademark Of The Manufacturing Organization, Its Address, The Full Name Of The Drug, The Date Of Manufacture, The Number Of The Series (Batch), Expiration Date, And Storage Conditions. The Shelf Life Is Not Less Than 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). Provision Of Documents Confirming The Quality Of The Drug, Erythritis Agar. For The Cultivation Of Brucella. Dry, Light Yellow, Powdery, In Plastic Bottles Of No More Than 0.25 Kg. A Label Is Pasted On The Vials, Which Indicates: The Manufacturers Organization, Its Address And Trademark, The Full Name Of The Drug, Its Composition, Series (Batch) Number, Date Of Manufacture, Expiration Date (Month, Hour), Weight Of The Drug, Storage Conditions. Instructions For Use (Preparation) In Russian And State Language Are Attached To Each Bottle. They Are Packed In Boxes With Thermal Insulation And Sealing Filling. The Shelf Life Is Not Less Than 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 ). Provision Of Documents Confirming The Quality Of The Drug., Campylobacagar. Nutrient Medium For Isolation And Cultivation Of Campylobacter. Packaged In Bottles Of No More Than 0.5 Kg. A Label Is Pasted On The Vials, Which Indicates: The Manufacturers Organization, Its Address And Trademark, The Full Name Of The Drug, Its Composition, Series (Batch) Number, Date Of Manufacture, Expiration Date (Month, Hour), Weight Of The Drug, Storage Conditions. Instructions For Use (Preparation) In Russian And State Language Are Attached To Each Bottle. They Are Packed In Boxes (Boxes) With Sealing Filling. The Shelf Life Is Not Less Than 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). Provision Of Documents Confirming The Quality Of The Drug. Additional Doses For Conducting Input Control From Each Series In The Amount Of One Packaging Unit., Pitatelnaya Sreda Of Levenstein-Jensen. To Isolate The Causative Agent Of Mycobacterium Tuberculosis And Atypical Mycobacteria From The Biological Material Under Investigation. Dry, Birch-Colored, Powdery In Bottles Of No More Than 0.25 Kg. A Label Is Affixed To The Bottles, Which Indicates: The Manufacturers Organization, Its Address And Trademark, The Full Name Of The Drug, Its Composition, Series (Batch) Number, Date Of Manufacture, Expiration Date (Months, Hours), Mass Of The Drug, Storage Conditions. Instructions For Use (Preparation) In Russian And State Language Are Attached To Each Bottle. They Are Packed In Boxes With Thermal Insulation And Sealing Filling. The Shelf Life Is Not Less Than 80% From The Date Of Manufacture To The Time Of Delivery (With A Shelf Life Of Twelve To Twenty-Four Months) And Not Less 60% From The Date Of Manufacture To The Time Of Delivery (With An Expiration Date Of More Than Twenty Four Months). Provision Of Documents Confirming The Quality Of The Drug.
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