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Advanced Contec Cms50-PRO Pulse Oximeter for Accurate SpO2 Monitoring
US$12.00
500-999 Pieces
US$7.00
1,000+ Pieces

Product profile

Customization

Available

Classification

Physiological Functions of Diagnosis and Monitoring Equipment

Type

Pulse Oximeter

Model NO.

CMS50-PRO

Certification

CE

Group

Middle-aged and Old

Weight

About 50g (Including Two AAA Batteries)

Function 1

Display of SpO2 Value,Pulse Rate Waveform

Function 2

Auto Power on, Auto Standby.

Indication

Low-Voltage Indication

Function 3

Capacity Pulse Scanning & Recording

Measurement

Oxygen Saturation, Pulse Rate

Transport Package

Carton

Specification

60(L)mm*30.5(W)mm*32.5 (H)mm

Trademark

CONTEC

Origin

China

HS Code

9018909911

Production Capacity

10000/Week

Key features

Advanced Measurement Tech: Employs Photoelectric Oxyhemoglobin and Capacity Pulse Scanning for accurate SpO2 and pulse rate.
Comprehensive Data Display: Shows SpO2, pulse rate, PI values, pulse waveform, and battery status with intuitive bar graphs.
Versatile Application Scenarios: Ideal for family, hospital, oxygen bars, community healthcare, and pre/post sports activities.
User-Friendly Features: Includes auto power on, auto standby, low-voltage warning, and optional sound prompts.
Compact and Portable Design: Lightweight at about 50g with dimensions 60x32.5x30.5mm, suitable for daily carrying.
CE Certified Quality: Meets CE certification standards for physiological diagnosis and monitoring equipment.

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: ≤3.05hTerms 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 technology does the CMS50-PRO use?
A:
It employs advanced Photoelectric Oxyhemoglobin Inspection Technology and Capacity Pulse Scanning & Recording Technology.
Q:Can the CMS50-PRO be used during strenuous exercise?
A:
No, it is designed for use before or after physical activities, not during strenuous exercises.
Q:What parameters can the device measure?
A:
It accurately measures oxygen saturation (SpO2) and pulse rate non-invasively via the finger.
Q:Does the device have a low-voltage warning?
A:
Yes, it features a low-voltage warning to prevent unexpected shutdowns.
Q:Is the CMS50-PRO CE certified?
A:
Yes, the device holds CE certification as a physiological function diagnosis and monitoring equipment.

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