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Medomics Fungal Fluorescent Staining Solution
Negotiable
3,000 Pieces

Product profile

Customization

Available

Certification

CE, ISO13485

Certificate

CE

Model NO.

Staining Solution

Transport Package

Box+Carton

Trademark

OBM/OEM

Origin

China

HS Code

3002150090

Key features

High Detection Accuracy: Improves detection rate and accuracy of positive pathogenic bacteria in clinical samples.
Clear Morphology Visualization: Makes morphology of epithelial cells, leukocytes, bacilli, cocci, molds and trichomoniasis clearly visible.
CE and ISO13485 Certified: Product holds CE certification and ISO13485 quality management system certification.
GMP Standard Production: Manufactured in over 10,000 square meters of GMP purification workshop meeting FDA, CE and CFDA standards.
Advanced R&D Technology: Features independent intellectual property in fluorescent staining and time-resolved immunofluorescence detection.
Professional Expert Team: Led by doctors from famous institutions including Osaka University and Zhejiang University.
Flexible Customization: Offers full customization, minor customization, and flexible customization from samples or designs.
Fast Lead Time: Average lead time within 15 workdays for both peak and off-peak seasons.

Company profile

Jiangsu Medomics Medical Technology Co., Ltd.
Importers and ExportersHigh Repeat Buyers ChoiceExperienced TeamExhibition Experience
CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service Available CertifiedCustomization Options: Customization from Samples, Customization from Designs, etc. CertifiedExport Year: 7 Years CertifiedNearest Port: Shanghai PortAverage Response Time: ≤18h

AI-Powered supplier vetting

SummaryJiangsu Medomics Medical Technology Co., Ltd. is an innovation-oriented medical-device enterprise in Nanjing engaged in the production and sale of biological and laboratory reagents, consumables, instruments, equipment, and medical devices. The supplier demonstrates broad customization and ODM capabilities, recent new-product development, OEM experience for well-known brands, raw-material traceability, and documented corrective-action and complaint-handling procedures. Its products are developed under ISO 13485 and have European CE certification. Service strengths include stocked inventory, stated lead times within 15 workdays in both peak and off-season periods, and participation in Medlab Middle East. Limitations include no valid manufacturing contract with related subcontractors, no overseas warehouse, showroom, agent, or branch, no overseas-service countries reported, and no available SDK. Financial credibility cannot be assessed from the provided information.
Supplier typeThe supplier is identified as a high-tech medical-device enterprise involved in R&D, production, and sales. Its stated business scope also covers biological and laboratory reagents, consumables, instruments, and equipment, subject to required regulatory approvals for applicable projects.
CertificationsThe supplier states that its product series were developed according to the ISO 13485 quality system and have European CE certification. This is explicit evidence of relevant quality-system and product-certification coverage.
After-Sales capabilityDocumented procedures and records exist for corrective and preventive actions and customer complaint handling. The supplier also reports inventory capability and lead times within 15 workdays in both peak and off-season, but has no overseas warehouse, showroom, agent, or branch and reports service coverage in zero countries.
R&D capabilityThe supplier reports new products during the past year, ODM capability, broad design and customization support, and an innovation-driven medical-device R&D profile. It also reports 42 years of total R&D-engineer experience, while no SDK is available; overall evidence supports strong product-development capability, with SDK capability specifically absent.
Production capacityEvidence includes production and sales operations, an automated processing line, raw-material traceability, four quality-assurance and quality-control inspectors, random finished-product inspection, stocked inventory, and stated lead times within 15 workdays. However, the supplier reports no valid manufacturing contract with its related subcontractors, which is a documented production-management weakness.
Customization capabilityThe supplier explicitly supports customization from samples, designs, full customization, minor customization, and flexible customization, and also provides ODM services. These statements directly demonstrate broad customization coverage.
Client casesThe supplier reports OEM service for well-known brands and participation in the Medlab Middle East offline trade show. These indicate some market-facing experience, but no specific customer names, project descriptions, order histories, or verifiable case details are provided.

Product Q&A

Q:What is the intended use of this solution?
A:
It is designed for fluorescent staining for fungal D-glucan detection and is for in vitro clinical diagnosis only.
Q:How should the staining solution be applied?
A:
Apply a drop directly to the sample to cover it, allow binding for 2 minutes, then cover with a coverslip and remove excess solution.
Q:What microscope settings are required?
A:
Use a biological fluorescent microscope with an excitation wavelength of 340nm-380nm and emission wavelength of 420nm-490nm.
Q:What are the storage precautions?
A:
Reagents must avoid fungal contamination and freezing is strictly prohibited.
Q:Who is qualified to operate this product?
A:
It should only be operated by personnel with professional experience or who are trained and qualified.

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