Catalogue values for High Performance Liquid Chromatography (HPLC) System

Category Specification Bid Requirement (Allowed Values)
Set 1 Number of samples the Analyser is capable to analyse (minimum), concurrently: 10, 50, 100, 150 Or higher
Availability of a bi-directional Laboratory Interface System (LIS): Yes, No
HPLC system have an inbuilt system check facility which checks that all the system parameters (eg, cartridge, buffer, reagent, waste etc) are ready before the sample analysis: Yes
HPLC system have a dual program mode to perform either HbA1c or HbA2/Hb F/HbA1c without changing any reagents or columns: Yes, No
HPLC system should not require changing of reagents while switching from HbA1c to HbA2/Hb F/HbA1c testing mode: Yes, No
HPLC System offers both NGSP & IFCC value reporting on the same patient report, control & calibrator report: Yes, No
If the HPLC system have feature of capillary collection kit for remote sample collection with sample stability at 2-8 degree C for 14 days: Yes, No
Certifications HPLC System is NGSP (National Glycohemoglobin Standardisation Program) Certified and traceable to IFCC reference method: Yes, No
Whether the product  is US FDA certified: Yes, No
Whether the product  is CE European certified: Yes