What is the lead time for delivery?

Within 15 workdays for both peak and off-peak seasons.

Ge M5s-D Ultrasound Probe Phased Array Heart Transducer for Logiq S8, Vivid E9

Name: Ge M5s-D Ultrasound Probe Phased Array Heart Transducer for Logiq S8, Vivid E9
Brand: Shenzhen Reyardmed Technology Limited.
SKU: 2090307072

Guangdong, ChinaShenzhen Reyardmed Technology Limited.

US$3,000.00-5,000.00

1 Piece

Product profile

Customization

Available

Customized

Certification

CE, FDA, ISO13485

Model NO.

M5S-D

Scale

Medium

Brand

Model

M5s-D

Type

Phased Array

Frequency

2.5MHz

Compatible Systems

Logiq S8, Vivid E9

Applications

Ob/Gyn, Msk, Gi

Materials

Metal, Pastics

Warranty

One Year

Transport Package

Common Box

Origin

China

HS Code

9018129190

Production Capacity

50000PCS/Year

Key features

CE Certification: Product meets CE safety and performance standards for medical devices.

One Year Warranty: Comprehensive one-year warranty covering mechanical defects and repairs.

Phased Array Technology: Advanced phased array design for high-resolution imaging in cardiac applications.

2.5MHz Frequency: Optimized 2.5MHz frequency for deep tissue penetration and clear imaging.

System Compatibility: Fully compatible with GE Logiq S8 and Vivid E9 ultrasound systems.

Multi-Application Support: Suitable for Ob/Gyn, Musculoskeletal (MSK), and Gastrointestinal (GI) exams.

Customized Options: Product specifications and features can be customized to specific needs.

ISO Certified Repair: Access to ISO-certified repair services with 100% quality guarantee.

Company profile

Shenzhen Reyardmed Technology Limited.

Guangdong, China

Business Type: Trading CompanyAverage Response Time: ≤2.41h

AI-Powered supplier vetting

SummaryThe supplier is a limited trading company offering ultrasound probes and related medical-device, technology, rental, consulting, and trading services. It reports ISO 13485 certification, 11–20 years of combined R&D-engineer experience, 6–10 quality-control staff, broad export coverage, and order fulfillment within 15 working days in both peak and off-peak periods. However, it does not provide OEM services for popular brands or an SDK, and the available quality-control evidence identifies zero quality-control test equipment, no written corrective/preventive-action or complaint-handling procedures, and unknown quality-assurance and traceability status. Financial records are referenced for 2022–2024, but no usable financial performance figures are provided. Customer relationships across multiple regions are described, but no specific customer cases are named.

CertificationsThe supplier reports holding ISO 13485 certification, a medical-device quality-management certification. The slices do not provide the certificate number, validity period, certification scope, or product coverage, so the certification is evidenced but its applicability cannot be fully assessed.

After-Sales capabilityThe supplier describes support from pre-sales consultation through after-sales technical assistance and states that it serves hospitals, clinics, and distributors internationally. However, it also reports no written procedures or records for corrective and preventive actions or customer-complaint handling, which shows a documented service-process deficiency despite the stated support commitment.

Production capacityThe supplier offers ultrasound probes, reports an annual production-output range, exports to multiple regions, and states order fulfillment within 15 working days in both peak and off-peak seasons. Against these positive operational indicators, the quality-control slice reports zero quality-control test equipment and unknown quality-assurance and traceability status, creating a clear documented weakness in production-quality infrastructure.

Customization capabilityThe supplier lists technology development, consultation, exchange, transfer, and technical services, and has reported R&D-engineer experience. However, it explicitly does not provide OEM services for popular brands and has no available SDK; no other product-customization process or capabilities are documented.