My-B016e Full Automatic Urine Dry Chemistry Analysis Auto Urinary Sediment Analyzer

Name: My-B016e Full Automatic Urine Dry Chemistry Analysis Auto Urinary Sediment Analyzer
Brand: Guangdong Maikang Medical Co., Ltd.
SKU: 1922337105

Guangdong, ChinaGuangdong Maikang Medical Co., Ltd.

US$24,943.00

1 Piece

Product profile

Customization

Available

Classification

Biological Diagnostics

Type

Urine Analyzer

Model NO.

MY-B016E

Group

All People

Product Name

Fully Automatic Assembly Line (Urinalysis Machine

Test Items

Classification and Quantitative Counting for Urine

Urine Dry Chemistry Analysis

Reflected Photoelectric Colorimetric Analysis

Function

Automatic Focus Calibration Without Focus Fluid

Feature

Automatic Urine Dry Chemical Detection and Microsc

Sample

Constant Speed 120 Samples/Hour

Counting Pool

Four-Channel

Application

Clinical Detection

Transport Package

Standard Export Packaging

Specification

160kg

Trademark

Mayamed

Origin

China

Production Capacity

10000PCS/Month

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: ≤5.92h

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.