Infectious Disease

Tetanus Antibody Rapid Test

Detects Clostridium tetani antibody. colloidal-gold. Specimen: Whole blood / Serum / Plasma.

Tetanus Antibody Rapid Test rapid diagnostic test — Progene Bio
Target / AnalyteClostridium tetani antibody
Disease / IndicationTetanus immunity
SeriesInfectious Disease
Methodcolloidal-gold
SpecimenWhole blood / Serum / Plasma
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 Clostridium tetani antibody in Whole blood / Serum / Plasma to support Tetanus immunity. 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 Clostridium tetani antibody.

Clinical Context

Tetanus antibody testing assesses immunity status.

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

Interpret with vaccination history.

Procurement

Specimen: Whole blood / Serum / Plasma. 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
IHP-302 H. pylori Antibody Rapid Test Cassette S / P Cassette 40 T CE
IHP-401 H. pylori Antibody Rapid Test Dipstick WB/S/P Dipstick 50T CE
IHP-402 H. pylori Antibody Rapid Test Cassette WB/S/P Cassette 40 T CE
ITE-402 Tetanus Rapid Test Cassette WB/S/P Cassette 40 T 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