What is the instrument classification?

It is classified as a Class II medical instrument.

What payment methods do you accept?

We accept T/T, L/C, D/P, D/A, MoneyGram, Credit Card, PayPal, Western Union, Cash, and Escrow.

What delivery terms are available?

We accept FOB, CFR, CIF, EXW, FAS, CIP, FCA, CPT, DEQ, DDP, DDU, Express Delivery, DAF, and DES.

Mindray Beneheart D3 Defibrilator Medical Aed Defibrillator

Name: Mindray Beneheart D3 Defibrilator Medical Aed Defibrillator
Brand: ICEN Medical Equipment Limited
SKU: 2064489065

Guangdong, ChinaICEN Medical Equipment Limited

US$1,000.00-9,000.00

1 Piece

Product profile

Customization

Available

Certification

CE, ISO13485

Group

All People

Model NO.

IN-D3

Transport Package

Carton Package

Trademark

ICEN

Origin

Guangzhou China

Production Capacity

2000 Sets/Month

Key features

CE and ISO13485 Certified: Meets international safety and quality standards for medical devices.

1-Year Warranty Coverage: Provides comprehensive protection against mechanical defects for one year.

Class II Medical Device: Categorized as a standard risk medical instrument for professional use.

Electric Power Source: Operates on electric power for reliable performance in medical settings.

Durable Metal and Plastic Build: Constructed with high-quality metal and plastic materials for longevity.

1-Year Shelf Life: Ensures product efficacy and safety within the designated storage period.

Global Export Experience: Over 8 years of experience exporting to more than 50 countries worldwide.

Comprehensive Payment Options: Accepts multiple currencies and payment methods including T/T, L/C, and PayPal.

Company profile

High Repeat Buyers ChoiceMulti-language PioneerIn-stock CapacityFast Delivery

ICEN Medical Equipment Limited

Guangdong, China

Business Type: Manufacturer/FactoryExport Year: 2017-10-01Average Response Time: ≤15hTerms of Payment: LC, T/T, D/P, etc.International Commercial Terms(Incoterms): FOB, EXW, CFR, CIF, DAT, FAS, DDP, DAP, CIP, CPT, Others, FCA

AI-Powered supplier vetting

SummaryICEN Technology Company Limited is identified as a China-based manufacturer/factory and limited company, although another record describes it as a trading company. It offers a broad range of medical equipment and reports OEM service for popular brands. The supplier holds ISO 9001 certification, has 6–10 quality-control staff and 6–10 R&D engineers, operates two production lines, and reports lead times within 15 workdays in both peak and off-peak seasons. R&D documentation is available for audit, but no SDK is available and the supplier reports zero R&D patents. It has inventory capacity and provides training, but lacks overseas agents or branches, overseas warehouses, overseas showrooms, and documented manufacturing-capacity contracts with affiliated subcontractors. Financial records are referenced for 2022–2024, but no financial performance details are provided. Customer project experience is described, including hospital design, equipment installation, and after-sales service, but no named customer...

CertificationsThe supplier reports ISO 9001 certification. An audit was conducted by BV, with a report period from 2025-10-23 to 2026-10-22, but the supplied audit result is recorded as 0 and no further interpretation or certification details are provided.

After-Sales capabilityThe supplier states that it provides equipment installation and after-sales service and lists training among its overseas service offerings. However, it has no overseas agents or branches, no overseas warehouse or showroom, and reports service coverage in zero countries, indicating that overseas service infrastructure is limited.

R&D capabilityThe supplier has 6–10 R&D engineers, uses PS and CAD software, operates production-line equipment, and can provide design input, output, review, verification, and validation documentation for audit. However, it reports zero R&D patents and no available SDK, so evidence supports operational R&D capability but not strong proprietary innovation.

Production capacityThe supplier operates two production lines, has 6–10 quality-control staff, reports lead times within 15 workdays during both peak and off-peak periods, and maintains in-stock capacity. Nevertheless, it has no valid manufacturing-capacity contract with affiliated subcontractors, which limits visibility into extended production resources.

Customization capabilityOEM service for popular brands is explicitly reported, and the supplier maintains R&D documentation covering design inputs, outputs, reviews, verification, and validation. These records support customization and product-development coordination, although no specific customized product examples are provided.