Development of Global Products and Commercialization of New Products
First written in FY2016. 17 of 19 entries say "Advanced", first in FY2017-Q2. Latest entry: 2026-07-30.
23 other companies' latest entry also says "Advanced".
- FY2026AdvancedAnnual report
「For urine test strips, we launched the “Fully Automated Urine Analyzer US-3600 (20-rack configuration)” in February 2026 as the successor to the “US-3500MS” fully automated urine analyzer.」
Launched the 20-rack version of US-3600 in February 2026 and advanced commercialization of a product supporting high-volume specimen setup, high-speed processing and direct sampling. - 2026-05-12AdvancedEarnings presentation
「Launch of the OC Sensor R70 fecal occult blood analyser」
The development and commercialisation plan for new products included a target launch for the OC Sensor R70 fecal occult blood analyser. - FY2025AdvancedAnnual report
「For urine test strips, we launched the compact, portable “US-1300” automated urine analyzer, the successor to US-1200, as the compact model in the US series in November 2024. In December 2024, we launched the fully automated “US-3600” urine analyzer, the successor to US-3500, as the flagship model in the US series.」
The company launched US-1300 and US-3600, successors to US-1200 and US-3500, respectively, advancing commercialization of new products. The launch and regulatory approval of MINtS-related products and antimicrobial susceptibility testing products were also reported. - FY2025-H1AdvancedAnnual report
「Sales of new rapid diagnostic kits, “ImmunoCatch–StrepA” and “ImmunoCatch–Adeno,” increased, bringing microbiological testing reagents to ¥2,194 million, up 3.0% year on year.」
Sales of the new rapid diagnostic kits “ImmunoCatch–StrepA” and “ImmunoCatch–Adeno” increased, advancing commercialization and sales of new products. - FY2023AdvancedAnnual report
「For OC-related reagents, we launched the OC-SENSOR Ceres fecal occult blood analyzer, which had obtained European IVDR certification, as well as fecal hemoglobin and fecal calprotectin assay reagents in November 2022. For latex reagents, we launched “LZ Test ‘Eiken’ CRP-RV” in February 2023. For immunochromatography reagents, we launched “Exdia EK Test Influenza A+B” in April 2022. For LAMP reagents, we launched the IVDR-compliant “Loopamp PURE DNA Extraction Kit” in July 2022.」
New products were launched and certifications obtained across multiple areas, including fecal occult blood, calprotectin, CRP, influenza, and IVDR-compliant LAMP products. - FY2022AdvancedAnnual report
「For products related to the novel coronavirus, in addition to the LAMP-based detection reagent launched in the previous fiscal year, we launched the portable immunofluorescence analyzer “Exdia TRF Plus,” based on time-resolved fluorescence immunoassay using the fluorescent substance europium, and the SARS coronavirus antigen kit “Exdia EK Test COVID-19 Ag” in March 2022.」
In addition to the LAMP-based detection reagent, the company launched a portable immunofluorescence analyzer and a SARS coronavirus antigen kit in March 2022. - FY2021AdvancedAnnual report
「In February 2021, we launched the “US-2300 Automated Urine Analyzer” and “OC-SENSOR Ceres Fecal Occult Blood Analyzer.”」
The US-2300 automated urine analyzer and OC-SENSOR Ceres fecal occult blood analyzer were launched in February 2021, advancing commercialization of new products. - FY2020AdvancedAnnual report
「To address the medical need of “Near the patient,” we developed a compact, fully automated genetic testing system using the LAMP method during the current consolidated fiscal year and launched the “Fully Automated Nucleic Acid Testing Instrument Simprova,” “Simprova Respiratory Infection Panel BP,LP,MP,” and “Simprova Extraction Kit/S1” in April 2020.」
The company developed a compact, fully automated genetic testing system and progressed through the launch of Simprova-related instruments, panels, and extraction kits. - FY2019AdvancedAnnual report
「In genetic testing reagents, we had already launched the European in vitro diagnostic “Loopamp MALARIA Pan/Pf Detection kit,” which simultaneously detects Plasmodium falciparum and all species of human malaria parasites, with the aim of overcoming malaria, one of the three major infectious diseases. In response to market demand for separate testing, we commercialized the two tests as separate kits. We also added “Loopamp MALARIA Pv detection kit,” which detects Plasmodium vivax, whose treatment differs from that for other malaria parasites, to the new product lineup.」
For malaria testing products, the existing simultaneous detection kit was commercialized as separate tests, and a kit for Plasmodium vivax was added to the lineup. - FY2018AdvancedAnnual report
「In genetic testing reagents, we launched “Loopamp Aspergillus F Detection Reagent Kit” as a research-use reagent in March 2018. The kit detects the gene of Aspergillus fumigatus, the principal causative organism of aspergillosis, which accounts for 70% of isolated Aspergillus species and is highly infectious and pathogenic. In bacteriological testing reagents, we launched the standard sheep blood agar medium “POURMEDIA Tryptic Soy 5% Sheep Blood Agar” in April 2017 and “POURMEDIA Vi Haemophilus Agar” in January 2018. In response to growing focus on antimicrobial resistance (AMR), we launched “KB Disk ‘Eiken’ Tigecycline” in October 2017 to support appropriate drug selection. In immunochromatography products, we launched “ImmunoCatch Noro Plus” in August 2017.」
New products were launched across multiple areas, including genetic testing, bacteriological testing, AMR measures, and immunochromatography, advancing commercialization. - FY2017AdvancedAnnual report
「Among rapid testing products based on immunochromatography, we launched “ImmunoCatch-Legionella” and “ImmunoCatch-Pneumococcus” overseas in October 2016. These products had been launched in Japan in December 2014 and January 2016, respectively, and had received favorable market responses. In addition, as measures to address antimicrobial resistance (AMR) have recently come into focus, we launched the antifungal susceptibility test “Yeast-like Fungi FP” in November 2016, the antimicrobial susceptibility test “Tigecycline FP” in November 2016, and “Metronidazole FP” in March 2017 to support the appropriate selection of antimicrobial drugs. For urinalysis instruments, we launched the portable “US-1200” automated urine analyzer, which supports a broad range of screening applications, in August 2016.」
The company launched rapid testing products overseas, 3 AMR-related susceptibility testing products, and the portable US-1200 automated urine analyzer, expanding the scope of its new product rollout. - FY2017-Q3AdvancedAnnual report
「We advanced product improvements through technological refinement and launched “US-1200,” the successor to the “US-1000” automated urine analyzer, in August 2016. In addition, “Loopamp Pertussis Detection Reagent Kit D,” a nucleic acid kit for Bordetella pertussis using the LAMP method, was listed for reimbursement in November 2016.」
The launch of US-1200 and reimbursement listing of LAMP-based Pertussis Detection Reagent Kit D advanced commercialization of new products. - FY2017-Q2AdvancedAnnual report
「We advanced product improvements through technological refinement and launched “US-1200,” the successor to the “US-1000” automated urine analyzer, in August 2016.」
The successor US-1200 was launched for an existing product, advancing commercialization of a new product. - FY2017-Q1RestatedAnnual report
「For rapid testing kits based on immunochromatography, we promoted sales mainly of “ImmunoCatch-Legionella” and “ImmunoCatch-Pneumococcus,” launched in January 2016, as part of the ImmunoCatch series.」
Sales promotion continued, centered on previously launched rapid testing kits. - FY2016First statedAnnual report
「We made the development of global products our highest priority, worked to understand market trends, strengthened and enhanced our existing lineup of major products, and advanced product development by strengthening our proprietary technologies and R&D capabilities.」
The company stated that it launched products for RSV, pneumococcus, Bordetella pertussis, KL-6 and other indications during the period.