Request For Quotation Purchase Of Medicines And Medical Products

Zotonic Solution Diluent (Rfid Lot 2304-894) For The Hematology Analyzer Of The Swelab Alfa Plus Series. The Volume Of One Bottle Is 20 Liters. Kit Contents: 1 X 20 L (At Least 900 Analysis Cycles). For Medicines And (Or) Medical Devices Imported And Produced On The Territory Of The Republic Of Kazakhstan Before The Expiration Of The Registration Certificate, The Following Are Submitted: Copies Of A Document Confirming Its Import Across The State Border Of The Republic Of Kazakhstan, Its Receipt By The Potential Supplier; Production By Domestic Producers, A Safety Report Issued In Accordance With The Procedure Established By Law. Mandatory Availability Of A Copy Of The Document On State Registration Of A Medicinal Product And (Or) Medical Device Or The Conclusion (Permission) Of The Authorized Body In The Field Of Healthcare For Import And Use In The Republic Of Kazakhstan., Lyse Solution (Rfid Lot 2303-888) For The Swelab Alfa Plus Series Hematology Analyzer. The Volume Of One Bottle Is 5 Liters. Kit Contents: 1 X 5 L (At Least 900 Analysis Cycles). For Medicines And (Or) Medical Devices Imported And Produced On The Territory Of The Republic Of Kazakhstan Before The Expiration Of The Registration Certificate, The Following Are Submitted: Copies Of A Document Confirming Its Import Across The State Border Of The Republic Of Kazakhstan, Its Receipt By The Potential Supplier; Production By Domestic Producers, A Safety Report Issued In Accordance With The Procedure Established By Law. Mandatory Availability Of A Copy Of The Document On State Registration Of A Medicinal Product And (Or) Medical Device Or The Conclusion (Permission) Of The Authorized Body In The Field Of Healthcare For Import And Use In The Republic Of Kazakhstan., Hematological Control Material 3-Level For Internal Quality Control According To Boule 3-Level Control (Normal, Low, High) For The Hematological Analyzer Swelab Alfa Plus (Control Blood). Catalog Number/Code 1504022-2. Set Contents: 1) 1 X 4.5 Ml – Low Level (Low); 2) 1 X 4.5 Ml – Normal Level (Normal); 3) 1 X 4.5 Ml – High Level (High). For Medicines And (Or) Medical Devices Imported And Produced On The Territory Of The Republic Of Kazakhstan Before The Expiration Of The Registration Certificate, The Following Are Submitted: Copies Of A Document Confirming Its Import Across The State Border Of The Republic Of Kazakhstan, Its Receipt By The Potential Supplier; Production By Domestic Producers, A Safety Report Issued In Accordance With The Procedure Established By Law. Mandatory Availability Of A Copy Of The Document On State Registration Of A Medicinal Product And (Or) Medical Device Or The Conclusion (Permission) Of The Authorized Body In The Field Of Healthcare For Import And Use In The Republic Of Kazakhstan.