IMPORTANT NOTE: These technical specifications are generic and may vary among suppliers.
Product name:
HIV (1+2) antibody (colloidal gold) Diagnostic Kit
Product code
Type of Immunoassay/ Analyte:
An in vitro, visually read test for the qualitative determination of antibodies against HIV-1 and HIV-2 in human
Name of reagent
Product code
Specimen of sample type to be used: serum, plasma, venous and capillary whole blood.
Accessories:
Coated well, Sample diluent, Conjugate, Conjugate Diluent, Anti-HIV-1 Positive Control, Anti-HIV-2 Positive Control, HIV-1 p24 Positive Control, Negative Control, Substrate Diluent, Substrate Concentrate, Wash Fluid
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: 30, 50s, 100s test pouch
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
Instructions for use
Transport Storage and operating Temperature:
Storage conditions: The test kit should be stored at 4-30°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 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
Product name:
HIV (1+2) antibody (colloidal gold) Diagnostic Kit
Product code
Type of Immunoassay/ Analyte:
An in vitro, visually read test for the qualitative determination of antibodies against HIV-1 and HIV-2 in human
Name of reagent
Product code
Specimen of sample type to be used: serum, plasma, venous and capillary whole blood.
Accessories:
Coated well, Sample diluent, Conjugate, Conjugate Diluent, Anti-HIV-1 Positive Control, Anti-HIV-2 Positive Control, HIV-1 p24 Positive Control, Negative Control, Substrate Diluent, Substrate Concentrate, Wash Fluid
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: 30, 50s, 100s test pouch
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
Instructions for use
Transport Storage and operating Temperature:
Storage conditions: The test kit should be stored at 4-30°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 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 10 | $5.58 |
| Pack of 25 | $13.75 |
| Pack of 40 | $17.73 |
| Pack of 50 | $27.14 |
| Pack of 100 | $65.00 |
