Infectious Disease

Giardia Rapid Test

Detects Giardia lamblia antigen. colloidal-gold. Specimen: Feces.

Giardia Rapid Test rapid diagnostic test — Progene Bio
Target / AnalyteGiardia lamblia antigen
Disease / IndicationGiardiasis
SeriesInfectious Disease
Methodcolloidal-gold
SpecimenFeces
Test time10–15 min (product-specific)
Storage2–30 °C, sealed pouch with desiccant
Shelf life24 months (product-specific)
RegulatoryNon-CE / registration in progress
OEM/ODMAvailable — private label & custom panel

Direct Answer

This rapid test detects Giardia lamblia antigen in Feces to support Giardiasis. It is a colloidal-gold screening test — a reactive result is presumptive and should be confirmed per the intended use.

Intended Use

Qualitative detection of Giardia lamblia antigen.

Clinical Context

Giardia is a common intestinal parasite causing diarrhea.

Test Principle

Colloidal-gold immunochromatography (lateral flow). The device captures the target analyte (antigen or antibody) on a membrane via labeled antibodies, producing a visible test line within minutes. Qualitative or semi-quantitative, intended as a screening/triage aid — not a replacement for confirmatory laboratory testing.

Limitations

Antigen detection indicates active infection.

Procurement

Specimen: Feces. Format: cassette. CE-marked line.

Interpretation

ResultLinesMeaning
PositiveTest + control lineTarget detected (presumptive positive)
NegativeControl line onlyBelow cut-off / not detected
InvalidNo control lineRepeat with a new device

Available SKUs (this series)

Cat. No.ProductSpecimenFormatKit SizeStatus
IGL-602 Giardia Lamblia Rapid Test Cassette Feces Cassette 10T CE
ICGC-625 Cryptosporidiumand Giardia LambliaCombo Rapid Test Cassette Feces Cassette 10T CE
IEGC-602 Entamoeba/Giardia/Crypto Rapid Test Cassette (1 Window) Feces Cassette 10T CE
IEGC-635 Entamoeba/Giardia/Crypto Combo Rapid Test Cassette (3 Windows) Feces Cassette 10T CE

Technical Evidence

Analytical performanceSensitivity, specificity, cut-off and precision are documented per product line in the datasheet and validation report.
Clinical performanceEvaluation data (study population, reference method, agreement) available on request.
Cross-reactivityDocumented per analyte — see limitations above.
DocumentsIFU · Datasheet · Certificate · Declaration of Conformity — request below.

Buyer Information

MOQProduct-dependent — low MOQ available on specialty assays
OEM / private labelCustom branding, cut-off, panel and packaging
SamplesAvailable for evaluation — request via RFQ
Lead timeOn request
DocumentsIFU · Datasheet · COA · Validation report · CE files · Registration support

Documentation & quotation — datasheet, IFU, certificate, MOQ and OEM/ODM options on request.

Request IFU / Spec Sheet Request Datasheet Request Certificate

Last reviewed: 2026-09-12