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Contec Ae1000A Hospital Equipment Arteriosclerosis Detector
US$3,000.00-7,000.00
1 Piece

Product profile

Customization

Available

Classification

Imaging Diagnostic Equipment

Type

Medical

Model NO.

AE1000A

Group

Middle-aged and Old

Transport Package

Carton

Trademark

CONTEC

Origin

China

Key features

Non-invasive Detection: Early screening of structural and functional lesions in human arterial blood vessels without invasion.
Dual Assessment Metrics: Calculates baPWV for vascular hardening and ABI for lower limb artery narrowing and blockage.
Automatic Report Generation: Generates ABI/PWV and exercise load reports automatically with clear, rich content results.
Comprehensive Data Management: Supports multiple checks per patient, appointment functionality, and easy case data review.
Multi-Disciplinary Application: Suitable for Cardiovascular Medicine, Health Examination, Vascular Surgery, Neurology, and more.
Portable & Lightweight: Compact host dimensions (248x163x57 mm) and lightweight design (approx. 1.7 kg) for convenience.
User-Friendly Operation: Convenient operation requiring no manual intervention after starting; diagnostic terms are editable.

Company profile

Contec Medical Systems Co., Ltd.
Importers and ExportersHigh Repeat Buyers ChoiceYears of Export ExperienceExperienced Team
Business Type: Manufacturer/FactoryExport Year: 1996-10-01Nearest Port: TianjinAverage Response Time: ≤2.68hTerms of Payment: LC, T/T, D/P, etc.International Commercial Terms(Incoterms): FOB, CFR, CIF

AI-Powered supplier vetting

SummaryThe supplier is a medical-device manufacturer and seller covering Class I, II, and III devices, medical cables, sensors, electronic products, and related software development. It demonstrates broad customization and ODM capabilities, reports new products in the past year, and has 719 R&D engineers. Production information includes 600,000 pieces each for pocket fetal dopplers and ECG machines, plus 40,000 patient monitors, although pulse oximeter output is not quantified. The supplier holds CE, ISO 9001:2015, and ISO 14001 certifications. Service systems include written supplier-management and corrective-action procedures, overseas warehouses and showrooms, and peak/off-season lead times within 15 workdays. Financial data is present for multiple years, but financial figures are excluded from this assessment. Evidence of customer cases includes OEM service for well-known brands, while there is no Fortune 500 collaboration and no available SDK.
Supplier typeThe supplier’s stated business scope covers production and sales of Class I, II, and III medical devices, medical cables, sensors, electronic products, and medical-device software development. This supports classification as a medical-device and related electronics manufacturer with design, assembly, sales, and technology-transfer activities.
CertificationsThe supplier reports CE product-compliance certification and ISO 9001:2015 and ISO 14001 management-system certifications. These explicitly demonstrate conformity and management-system credentials, although no additional certification scope or certificate validity details are provided.
After-Sales capabilityThe supplier reports written service-capability procedures with followed records, a corrective and preventive action mechanism, and average lead times within 15 workdays in both off-season and peak season. It also provides overseas debugging, maintains an overseas warehouse and showroom, and participates in offline trade shows, but has no overseas agents or branches and reports service coverage in zero countries.
R&D capabilityThe supplier reports new products during the past year, ODM capability, medical-device software development and technology transfer, and 719 R&D engineers. However, it has no available SDK, so the evidence supports strong product-development resources but not a complete software-development ecosystem.
Production capacityReported annual output includes 600,000 pocket fetal dopplers, 40,000 patient monitors, and 600,000 ECG machines, supported by automatic programming, chip-mounting, reflow-soldering, and wave-soldering equipment. The supplier also reports a broad medical-device manufacturing scope and lead times within 15 workdays in both seasons, although pulse-oximeter volume is not quantified.
Customization capabilityThe supplier explicitly offers customization from samples, customization from designs, full customization, minor customization, and flexible customization. These capabilities are stated both under R&D and design-services information, indicating broad customization coverage rather than a single limited option.
Client casesThe supplier reports OEM service for well-known brands and a repeat-buyer preference of 50%–80%, providing evidence of prior branded-customer and repeat-business experience. However, it reports no collaboration with Fortune 500 companies, and no specific customer names or project examples are provided.

Product Q&A

Q:What is the primary function of the AE1000A?
A:
It is a non-invasive hemodynamic testing device used for early screening of structural and functional lesions in human arterial blood vessels.
Q:How does the device assess vascular health?
A:
It collects ECG, heart sounds, and pulse wave signals to calculate baPWV for vascular hardening, and measures limb blood pressure to calculate ABI for artery narrowing.
Q:What types of reports does the device generate?
A:
It automatically generates ABI/PWV reports and exercise load reports, which are rich in content and provide clear diagnostic results.
Q:Which medical departments can use this equipment?
A:
It is applicable in Cardiovascular Medicine, Health Examination Centers, Vascular Surgery, Endocrinology, Neurology, and Hypertension Departments.
Q:Is the operation of the AE1000A complex?
A:
No, it features convenient operation with no manual intervention required after starting, and it automatically generates reports and diagnostic results.

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