Urea-03, 60Ml. With An Expiration Date Of At Least May 2027. List Of Documents That Are Required Upon Receipt Of Medicines, Medical Devices, Reagents: - Certificate Of Product Conformity (Upon Declaration), Certifying That The Given Drug, Medical Device, Reagent Have Passed The Quality Assessment; - Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug, Medical Device, Reagent Is Registered And Approved For Use On The Territory Of The Republic Of Kazakhstan. If A Medicine, Medical Device, Or Reagent Is Not Registered In The Republic Of Kazakhstan, Then An Import Permit Is Required., Immersion Oil For Microscopy Type A 100 Ml (For Leukemia, Gynecological Smears). With An Expiration Date Of At Least December 2027. List Of Documents That Are Required Upon Receipt Of Medicines, Medical Devices, Reagents: - Certificate Of Product Conformity (Upon Declaration), Certifying That The Given Drug, Medical Device, Reagent Have Passed The Quality Assessment; - Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug, Medical Device, Reagent Is Registered And Approved For Use On The Territory Of The Republic Of Kazakhstan. If A Medicine, Medical Device, Or Reagent Is Not Registered In The Republic Of Kazakhstan, Then An Import Permit Is Required., Hematological Reagent Lysis Solution Cellclean (Cleansing Solution 50 Ml). With An Expiration Date Of At Least February 2027. List Of Documents That Are Required Upon Receipt Of Medicines, Medical Devices, Reagents: - Certificate Of Product Conformity (Upon Declaration), Certifying That The Given Drug, Medical Device, Reagent Have Passed The Quality Assessment; - Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug, Medical Device, Reagent Is Registered And Approved For Use On The Territory Of The Republic Of Kazakhstan. If A Medicine, Medical Device, Or Reagent Is Not Registered In The Republic Of Kazakhstan, Then An Import Permit Is Required., A Set Of Reagents For Determining The Concentration Of Total Cholesterol In Human Serum (Plasma) Using The Enzymatic Colorimetric Method “Cholesterol-12”. With An Expiration Date Of No Less Than May 2027. List Of Documents That Are Required Upon Receipt Of Medicines, Medical Devices, Reagents: - Certificate Of Product Conformity (Upon Declaration), Certifying That The Given Drug, Medical Device, Reagent Have Passed The Quality Assessment; - Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug, Medical Device, Reagent Is Registered And Approved For Use On The Territory Of The Republic Of Kazakhstan. If A Medicine, Medical Device, Or Reagent Is Not Registered In The Republic Of Kazakhstan, Then An Import Permit Is Required., Azur-Eosin According To Romanovsky, Is Intended For Staining Blood Cells.1.00. With An Expiration Date Of At Least February 2027. List Of Documents That Are Required Upon Receipt Of Medicines, Medical Devices, Reagents: - Certificate Of Product Conformity (Upon Declaration), Certifying That The Given Drug, Medical Device, Reagent Have Passed The Quality Assessment; - Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug, Medical Device, Reagent Is Registered And Approved For Use On The Territory Of The Republic Of Kazakhstan. If A Medicine, Medical Device, Or Reagent Is Not Registered In The Republic Of Kazakhstan, Then An Import Permit Is Required., Dye-Fixer Eosin Methylene Blue According To May-Grunwald. Fixative-Dye According To May-Grunwald In Solution, Intended For Use As A Fixative And Dye Of Blood Cells. 100 Ml*2 Vital. With An Expiration Date Of At Least February 2027. List Of Documents That Are Required Upon Receipt Of Medicines, Medical Devices, Reagents: - Certificate Of Product Conformity (Upon Declaration), Certifying That The Given Drug, Medical Device, Reagent Have Passed The Quality Assessment; - Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug, Medical Device, Reagent Is Registered And Approved For Use On The Territory Of The Republic Of Kazakhstan. If A Medicine, Medical Device, Or Reagent Is Not Registered In The Republic Of Kazakhstan, Then An Import Permit Is Required., Isotonic Diluent Cellpak 20 L Included In The Kit, Automatic Hematology Analyzer. With An Expiration Date Of At Least September 2027. List Of Documents That Are Required Upon Receipt Of Medicines, Medical Devices, Reagents: - Certificate Of Product Conformity (Upon Declaration), Certifying That The Given Drug, Medical Device, Reagent Have Passed The Quality Assessment; - Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug, Medical Device, Reagent Is Registered And Approved For Use On The Territory Of The Republic Of Kazakhstan. If A Medicine, Medical Device, Or Reagent Is Not Registered In The Republic Of Kazakhstan, Then An Import Permit Is Required., Isotonic Diluent Cellpak 20 L Included In The Kit, Automatic Hematology Analyzer. With An Expiration Date Of At Least February 2027. List Of Documents That Are Required Upon Receipt Of Medicines, Medical Devices, Reagents: - Certificate Of Product Conformity (Upon Declaration), Certifying That The Given Drug, Medical Device, Reagent Have Passed The Quality Assessment; - Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug, Medical Device, Reagent Is Registered And Approved For Use On The Territory Of The Republic Of Kazakhstan. If A Medicine, Medical Device, Or Reagent Is Not Registered In The Republic Of Kazakhstan, Then An Import Permit Is Required., Cardiolipin Antigen For Microprecipitation Reaction (100 Ml*2). With An Expiration Date Of At Least February 2027. List Of Documents That Are Required Upon Receipt Of Medicines, Medical Devices, Reagents: - Certificate Of Product Conformity (Upon Declaration), Certifying That The Given Drug, Medical Device, Reagent Have Passed The Quality Assessment; - Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug, Medical Device, Reagent Is Registered And Approved For Use On The Territory Of The Republic Of Kazakhstan. If A Medicine, Medical Device, Or Reagent Is Not Registered In The Republic Of Kazakhstan, Then An Import Permit Is Required., Control Blood For The Sysmex Hematology Analyzer. List Of Documents That Are Required Upon Receipt Of Medicines, Medical Devices, Reagents: - Certificate Of Product Conformity (Upon Declaration), Certifying That The Given Drug, Medical Device, Reagent Have Passed The Quality Assessment; - Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug, Medical Device, Reagent Is Registered And Approved For Use On The Territory Of The Republic Of Kazakhstan. If A Medicine, Medical Device, Or Reagent Is Not Registered In The Republic Of Kazakhstan, Then An Import Permit Is Required., Isotonic Diluent Cellpak 20 L Included In The Kit, Automatic Hematology Analyzer. With An Expiration Date Of At Least May 2027. List Of Documents That Are Required Upon Receipt Of Medicines, Medical Devices, Reagents: - Certificate Of Product Conformity (Upon Declaration), Certifying That The Given Drug, Medical Device, Reagent Have Passed The Quality Assessment; - Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug, Medical Device, Reagent Is Registered And Approved For Use On The Territory Of The Republic Of Kazakhstan. If A Medicine, Medical Device, Or Reagent Is Not Registered In The Republic Of Kazakhstan, Then An Import Permit Is Required., A Set Of Reagents For Determining The Concentration Of Total And Direct Bilirubin In Blood Serum Using The Unified Jendrassik-Grof Method “Bilirubin-12-Vital”. With An Expiration Date Of At Least February 2027. List Of Documents That Are Required Upon Receipt Of Medicines, Medical Devices, Reagents: - Certificate Of Product Conformity (Upon Declaration), Certifying That The Given Drug, Medical Device, Reagent Have Passed The Quality Assessment; - Registration Certificate Of The Republic Of Kazakhstan, Certifying That This Drug, Medical Device, Reagent Is Registered And Approved For Use On The Territory Of The Republic Of Kazakhstan. If A Medicine, Medical Device, Or Reagent Is Not Registered In The Republic Of Kazakhstan, Then An Import Permit Is Required.
