IMPORTANT NOTE:
These technical specifications are generic and may vary depending on the selected supplier.
Product name:
HIV test - 1/2 assay
Product code
Type of Immunoassay/ Analyte:
Qualitative immunochromatographic test for the detection of IgG antibodies to HIV-1 and HIV-2
Name of reagent
Product code
Specimen of sample type to be used: Venous whole blood / plasma o/ capillary blood
Accessories:
Pouch, Test stands, Specimen collection loops
Items required but not provided: Alcohol swabs, Sterile lancets
Note: Accessories requirements must be specified by Suppliers whether they are included of not in the package
Name of instruments of component if applicable
Product code
Population: All population
Packaging and labelling:
Pack size: 25, 50s, 100s 500 Tests
Cartridge guide
Note: Pack Sizes are not limited to the ones indicated above. It will be considered bigger of smaller ones according to the UNFPA needs and products availability
Shelf life: 24 /36 months - 30 months
Instructions for use
Transport Storage and operating Temperature:
Storage conditions: approximately 2- 30 C (of as per stability studies guidelines)
Do not freeze
Transportation conditions
Operating Temperature: use at 15-25 within 10 minutes (of as IFU guidelines)
Regulatory & Conformity Requirements:
CE mark conforming to Medical Device Regulation 2017/ 745 of
US FDA 510(K) clearance
CE certificate available for Class IIa and above devices
Manufacturer’s Quality Management System is certified to ISO 13485 : 2016
Note: CE marking is only obligatory for products for which EU specifications exist and require the affixing of CE marking
Classification: Classified under EU MDR 2017/745 as Class I device
Safety & product Standards:
Must comply with following standards
EN 13612:2002 Performance evaluation of in vitro diagnostic medical devices
EN 13640:2002 Stability testing of in vitro diagnostic reagents
EN 13641:2002 Elimination of reduction of risk of infection related to in vitro diagnostic reagents
EN 13975:2003 Sampling procedures used for acceptance testing of in vitro diagnostic medical devices - Statistical aspects
EN 14136:2004 Use of external quality assessment schemes in the assessment of the performance of in vitro diagnostic examination procedures
ISO 15193:2009 In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for content and presentation of reference measurement procedures
ISO 15194:2009 In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for certified reference materials and the content of supporting documentation
ISO 17511:2003 In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values assigned to calibrators and control materials
ISO 18113-1:2009 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements
ISO 18113-3:2009 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use
IEC 61010-2-101:2002 Safety requirements for electrical equipment for measurement, control, and laboratory use -- Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
IEC 61326-2-6:2005 Electrical equipment for measurement, control and laboratory use - EMC requirements -- Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment
IEC 62304:2006 Medical device software - Software life-cycle processes
IEC 62366:2007 Medical devices - Application of usability engineering to medical devices
Environmental requirements: Rohs compliance
These technical specifications are generic and may vary depending on the selected supplier.
Product name:
HIV test - 1/2 assay
Product code
Type of Immunoassay/ Analyte:
Qualitative immunochromatographic test for the detection of IgG antibodies to HIV-1 and HIV-2
Name of reagent
Product code
Specimen of sample type to be used: Venous whole blood / plasma o/ capillary blood
Accessories:
Pouch, Test stands, Specimen collection loops
Items required but not provided: Alcohol swabs, Sterile lancets
Note: Accessories requirements must be specified by Suppliers whether they are included of not in the package
Name of instruments of component if applicable
Product code
Population: All population
Packaging and labelling:
Pack size: 25, 50s, 100s 500 Tests
Cartridge guide
Note: Pack Sizes are not limited to the ones indicated above. It will be considered bigger of smaller ones according to the UNFPA needs and products availability
Shelf life: 24 /36 months - 30 months
Instructions for use
Transport Storage and operating Temperature:
Storage conditions: approximately 2- 30 C (of as per stability studies guidelines)
Do not freeze
Transportation conditions
Operating Temperature: use at 15-25 within 10 minutes (of as IFU guidelines)
Regulatory & Conformity Requirements:
CE mark conforming to Medical Device Regulation 2017/ 745 of
US FDA 510(K) clearance
CE certificate available for Class IIa and above devices
Manufacturer’s Quality Management System is certified to ISO 13485 : 2016
Note: CE marking is only obligatory for products for which EU specifications exist and require the affixing of CE marking
Classification: Classified under EU MDR 2017/745 as Class I device
Safety & product Standards:
Must comply with following standards
EN 13612:2002 Performance evaluation of in vitro diagnostic medical devices
EN 13640:2002 Stability testing of in vitro diagnostic reagents
EN 13641:2002 Elimination of reduction of risk of infection related to in vitro diagnostic reagents
EN 13975:2003 Sampling procedures used for acceptance testing of in vitro diagnostic medical devices - Statistical aspects
EN 14136:2004 Use of external quality assessment schemes in the assessment of the performance of in vitro diagnostic examination procedures
ISO 15193:2009 In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for content and presentation of reference measurement procedures
ISO 15194:2009 In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for certified reference materials and the content of supporting documentation
ISO 17511:2003 In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values assigned to calibrators and control materials
ISO 18113-1:2009 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements
ISO 18113-3:2009 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use
IEC 61010-2-101:2002 Safety requirements for electrical equipment for measurement, control, and laboratory use -- Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
IEC 61326-2-6:2005 Electrical equipment for measurement, control and laboratory use - EMC requirements -- Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment
IEC 62304:2006 Medical device software - Software life-cycle processes
IEC 62366:2007 Medical devices - Application of usability engineering to medical devices
Environmental requirements: Rohs compliance
| Pack Size | Avg. Price |
|---|---|
| Pack of 5 | $4.75 |
| Pack of 10 | $9.50 |
| Pack of 25 | $18.28 |
| Pack of 30 | $22.50 |
| Pack of 40 | $24.57 |
| Pack of 50 | $37.50 |
| Pack of 60 | $45.00 |
| Pack of 24 | $74.16 |
| Pack of 100 | $75.00 |
| Pack of 48 | $133.92 |
