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 | |