Urea-03, 60Ml. With A Shelf Life Of At Least December 2026. A List Of Documents That Are Necessary For The Receipt Of Medicines, Medical Devices, Reagents: A Certificate Of Conformity Of Products (When Declared) Certifying That This Drug, Mi, Reagent Have Passed Quality Assessment; The Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug, Mi, The Reagent Is Registered And Allowed For Use In The Territory Of The Republic Of Kazakhstan. If The Drug, Medical Product, Reagent Is Not Registered In The Republic Of Kazakhstan, Then Permission To Import., A Set Of Reagents To Determine The Concentration Of The General And Direct Bilirubin In The Blood Serum With A Unified Method Of Yendrasic-Graph Bilirubin-12-Vital. With A Shelf Life Of At Least December 2026. A List Of Documents That Are Necessary For The Receipt Of Medicines, Medical Devices, Reagents: A Certificate Of Conformity Of Products (When Declared) Certifying That This Drug, Mi, Reagent Have Passed Quality Assessment; The Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug, Mi, The Reagent Is Registered And Allowed For Use In The Territory Of The Republic Of Kazakhstan. If The Drug, Medical Product, Reagent Is Not Registered In The Republic Of Kazakhstan, Then Permission To Import., Control Blood For The Hematological Analyzer Sysmex. A List Of Documents That Are Necessary For The Receipt Of Medicines, Medical Devices, Reagents: A Certificate Of Conformity Of Products (When Declared) Certifying That This Drug, Mi, Reagent Have Passed Quality Assessment; The Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug, Mi, The Reagent Is Registered And Allowed For Use In The Territory Of The Republic Of Kazakhstan. If The Drug, Medical Product, Reagent Is Not Registered In The Republic Of Kazakhstan, Then Permission To Import., A Set Of Reagents To Determine The Content Of The Total Protein In Serum (Plasma) Of Human Blood By The Biuret Method “General Protein-01” 2X100 Ml. With A Shelf Life Of At Least December 2026. A List Of Documents That Are Necessary For The Receipt Of Medicines, Medical Devices, Reagents: A Certificate Of Conformity Of Products (When Declared) Certifying That This Drug, Mi, Reagent Have Passed Quality Assessment; The Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug, Mi, The Reagent Is Registered And Allowed For Use In The Territory Of The Republic Of Kazakhstan. If The Drug, Medical Product, Reagent Is Not Registered In The Republic Of Kazakhstan, Then Permission To Import.
