CanAg SCC EIA

Enzyme immunoassay test kits developed for clinical diagnostic applications. These assays provide reliable immunological detection across various medical testing scenarios.

Enzyme immunoassay tests for diagnostic purposes, part of Reagena's comprehensive product portfolio for detecting animal-borne infections.

Manual or semi-automated immunoassay kit for cancer antigen detection. Used for oncology diagnostics and tumor marker measurement.

An in vitro diagnostic reagent used as an aid in evaluating the severity of atopic dermatitis in children aged 15 years and below.

CE IVD certified genetic testing kits for diagnostic and screening purposes across multiple genetic conditions. Meets European regulatory requirements for in vitro diagnostic medical devices.

Comprehensive immunodiagnostic test kits designed to detect and identify infectious disease markers. Manufactured internally with CE certification for clinical laboratory use.

An in vitro diagnostic rapid test kit for the detection of carcinoembryonic antigen (CEA). The product is supplied in a kit format containing 100 test strips per package. It is manufactured by Asan Pharmaceutical Co., Ltd for human medical diagnostics.

A rapid diagnostic test kit certified under EU IVDR regulations for self-testing applications. Designed for point-of-care testing with fluorescence chromatography or latex turbidity platforms.

A cervical cytology immunochemistry detection kit for human papillomavirus (HPV) E7 protein testing. The kit uses mouse monoclonal antibodies with high specificity and affinity to detect E7 protein expression in cervical cells through immunochemical staining. Available in multiple volumes (3 mL, 6 mL, 9 mL, 12 mL per tube), it is designed for preliminary screening of cervical intraepithelial lesions and can identify early-stage cervical lesions, high-grade lesions, and assist clinicians in providing accurate diagnostic information while reducing unnecessary cervical biopsies.

An in vitro diagnostic rapid test kit for the detection of carcinoembryonic antigen (CEA). The product is supplied in a kit format containing 25 test strips per package. It is manufactured by Asan Pharmaceutical Co., Ltd for human medical diagnostics.

Diagnostic test device bearing CE certification mark for use in European medical markets. Demonstrates compliance with European regulatory requirements for in vitro diagnostics.

CE-IVD marked qPCR kits for molecular diagnostics in oncology, infection detection, antimicrobial resistance, and genetic testing. Kits include all reagents with internal controls and are validated on multiple real-time PCR platforms. Assays designed to CDC and WHO standards offer high sensitivity and specificity with simplified setup and data analysis.