What analysis parameters are provided?

It provides distribution curves, dynamic trajectories, motility speed, energy isarithmic maps, and detailed morphology counts.

What is the lead time for production?

The average lead time is within 15 workdays for both peak and off seasons.

My-B041c-1 Human Sperm Analysis Machine with Disposable Sperm Counting Chamber Clinic Sperm Analyzer

Name: My-B041c-1 Human Sperm Analysis Machine with Disposable Sperm Counting Chamber Clinic Sperm Analyzer
Brand: Guangdong Maikang Medical Co., Ltd.
SKU: 2210165385

Guangdong, ChinaGuangdong Maikang Medical Co., Ltd.

US$5,470.00

1-9 Pieces

US$4,376.00

10+ Pieces

Product profile

Customization

Available

Certification

ISO13485

Scale

Medium

Model NO.

MY-B041C-1

Keyword

Sperm Quality Analyzer

Detected Sperms

More Than 1000

The Range of Detection Speed

0-180µm/S

MOQ

Transport Package

Sperm Quality Analyzer Packing

Trademark

MAYAMED

Origin

China

Key features

Comprehensive Analysis: Analyzes motility, morphology, and provides dynamic trajectory curves.

ISO13485 Certified: Manufactured under strict ISO13485 quality management standards.

Flexible Customization: Supports full customization, minor customization, and design-based options.

Detailed Morphology: Identifies head, tail, body, and mixed teratosperm counts accurately.

Fast Processing: Analysis time ranges from 1-5 seconds for efficient clinical use.

OEM/ODM Support: Manufacturer offers both OEM and ODM services for tailored solutions.

Multi-Parameter Output: Outputs technical data, histograms, and patient case management info.

Company profile

Years of Export ExperienceExhibition ExperienceIn-stock CapacityPrivate Mold

Guangdong Maikang Medical Co., Ltd.

Guangdong, China

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: 12 years CertifiedNearest Port: Guangzhou Port, Shenzhen PortAverage Response Time: ≤5.26h

AI-Powered supplier vetting

SummaryThe supplier is a combined company with over 10 years of experience, reported exports to more than 100 countries, and stated concentration in African, Middle Eastern African, and South American markets. It demonstrates broad customization, active R&D, ODM and OEM capabilities, R&D documentation, and production of medical equipment at 100,000 pieces annually. Manufacturing resources include three production lines, listed processing equipment, valid contracts with associated subcontractors, and in-stock capacity. Service management procedures cover supplier assessment, corrective and preventive actions, and customer complaints. However, the evidence does not establish certification holdings, and the supplier reports no R&D patents, no SDK, no overseas warehouse, no overseas showroom, and no overseas agents or branches. Financial credibility cannot be determined from the provided year references alone. Customer-case evidence is limited to general export and brand-service claims without named customers or...

After-Sales capabilityThe supplier states that it has an after-sale service office in Lagos, Nigeria and Madagascar, while also maintaining written and followed procedures for customer complaints and service corrective actions. However, another record states it has no overseas agents or branches and lists overseas service offerings as training, so the overall overseas service structure is inconsistently documented.

R&D capabilityThe supplier reports new products within the past year, ODM capability, and auditable R&D design-input, output, review, verification, and validation documentation. It has two R&D engineers and uses PS and CAD, but reports zero patents and no available SDK, indicating documented product-development capability without evidence of patent-based innovation or SDK support.

Production capacityThe supplier reports annual medical-equipment output of 100,000 pieces, three production lines, listed machining and production equipment, in-stock capacity, and valid manufacturing contracts with associated subcontractors. These statements provide explicit evidence of established production capacity.

Customization capabilityBoth R&D and design-capability records list customization from samples, designs, full customization, minor customization, and flexible customization. This directly supports a broad range of customization services.