Infectious Disease

Dengue IgG/IgM Rapid Test

Detects Dengue IgG/IgM. colloidal-gold. Specimen: WB / S / P.

Target / Analyte	Dengue IgG/IgM
Disease / Indication	Dengue
Series	Infectious Disease
Method	colloidal-gold
Specimen	WB / S / P
Test time	10–15 min (product-specific)
Storage	2–30 °C, sealed pouch with desiccant
Shelf life	24 months (product-specific)
Regulatory	CE (IVDD 98/79/EC)
OEM/ODM	Available — private label & custom panel

Direct Answer

This rapid test detects Dengue IgG/IgM in WB / S / P to support Dengue. 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 Dengue IgM and IgG antibodies for serological diagnosis of dengue.

Clinical Context

IgM appears ~3–5 days after fever onset; IgG indicates past exposure or secondary infection. Combined IgM/IgG is standard for late-acute and convalescent dengue serology.

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

Cross-reactivity with Zika and other flaviviruses is possible; interpret serology with travel and vaccination history.

Procurement

Specimen: whole blood / serum / plasma. Format: cassette. CE-marked line.

Interpretation

Result	Lines	Meaning
Positive	Test + control line	Target detected (presumptive positive)
Negative	Control line only	Below cut-off / not detected
Invalid	No control line	Repeat with a new device

Common misconception

A negative rapid test does not always exclude infection — timing, specimen and pathogen load all matter. Follow up clinically where suspicion is high.

Sources

Screening results are presumptive, not diagnostic. Confirmatory testing follows WHO, CDC and national regulatory guidance — see screening vs confirmatory.

Available SKUs (this series)

Cat. No.	Product	Specimen	Format	Kit Size	Status
ICHI-302	Chikungunya IgG/IgM Rapid Test Cassette	S/P	Cassette	40 T	CE
ICHI-402	Chikungunya IgG/IgM Rapid Test Cassette	WB/S/P	Cassette	40 T	CE
IDEN-402	Dengue IgG/IgM Rapid Test Cassette	WB/S/P	Cassette	10 T	CE
IDES-402	Dengue NS1 Rapid Test Cassette	WB/S/P	Cassette	10 T	CE
IDEC-425	Dengue IgG/IgM And NS1 Combo Rapid Test Cassette	WB/S/P	Cassette	25 T	CE
IZIB-402	Zika IgG/IgM Rapid Test Cassette	WB/S/P	Cassette	10T	CE
IZIC-425	Zika IgG/IgM and NS1 Combo Rapid Test Cassette	WB/S/P	Cassette	10T	CE
IFIL-302	Filariasis IgG/IgM Rapid Test Cassette	S / P	Cassette	40 T	CE
IFIL-402	Filariasis IgG/IgM Rapid Test Cassette	WB/S / P	Cassette	40 T	CE
ITY-302	Typhoid IgG/IgM Rapid Test Cassette	S / P	Cassette	40 T	CE
ITY-402	Typhoid IgG/IgM Rapid Test Cassette	WB/S/P	Cassette	40 T	CE
ITY-401	Typhoid IgG/IgM Rapid Test Dipstick	WB/S/P	Dipstick	50 T	CE

Technical Evidence

Analytical performance	Sensitivity, specificity, cut-off and precision are documented per product line in the datasheet and validation report.
Average accuracy	≥96% (overall agreement rate, manufacturer-validated). Per-product sensitivity and specificity are documented in the datasheet.
Clinical performance	Evaluation data (study population, reference method, agreement) available on request.
Cross-reactivity	Documented per analyte — see limitations above.
Documents	IFU · Datasheet · Certificate · Declaration of Conformity — request below.

Buyer Information

MOQ	Product-dependent — low MOQ available on specialty assays
OEM / private label	Custom branding, cut-off, panel and packaging
Samples	Available for evaluation — request via RFQ
Lead time	On request
Documents	IFU · Datasheet · COA · Validation report · CE files · Registration support

Related knowledge

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