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DBP-1313
Joytech / OEM
The Joytech DBP-1313 is an electronic blood pressure monitor designed for professional reliability and universal ease of use. It has obtained core global market access and quality certifications including US FDA, EU MDR CE, and ISO13485 Quality Management System, establishing a dual trust foundation suitable for both home and clinical settings. The device combines an extra-large display, multi-user data management, and multiple practical functions, supporting flexible power options. It aims to provide users with a clear, convenient, and accurate health monitoring experience from measurement to storage.
1. The product's core advantage lies in its comprehensive international compliance. Holding FDA, MDR CE, and ISO13485 certifications simultaneously means the device meets the regulatory requirements of stringent markets like the US and EU in design, production, and performance. This makes it suitable not only for daily home monitoring but also as a reliable auxiliary tool in professional medical settings such as clinics and pharmacies, providing purchasers with a broad market access pass.
2. The device is equipped with an extra-large display, making readings clear and prominent, greatly facilitating users of all ages, especially in low-light conditions. Its structure of 4 independent memory groups (30 records each) can meet the basic data tracking needs of multiple family members or patients. Each record includes a date and time stamp for easy review and comparison.
3. Centered on reliability and usability, the DBP-1313 incorporates multiple safeguards: Intelligent Digital Error Messages visually indicate operational issues like improper cuff placement; Low Battery Detection and Auto Power-Off functions effectively manage energy consumption, preventing battery drain or waste. These details collectively ensure the device is always in optimal ready-to-use condition.
4. The product form fully considers flexibility. It supports dual power modes via AC adapter or Micro USB, allowing users to choose between batteries or connecting to a power source/power bank based on the scenario. The included deluxe carry case provides proper protection for the device, cuff, and accessories, making it very convenient for home storage, travel, or healthcare workers making house calls.
Digital error messages
Extra large display
4×30 memories with date and time
Deluxe carry case
AC adapter port or micro USB
Automatic power-off
Model | DBP-1313 |
Type | Up-Arm |
Measurement Method | Oscillometric Method |
Pressure Range | 0 to 300mmHg |
Pulse Range | 30 to 180 Beat/ Minute |
Pressure Accuracy | ±3mmHg |
Pulse Accuracy | ±5% |
Display Size | 5.5x8.4cm |
Memory Bank | 4x30 |
Date & Time | Month+Day+Hour+Minute |
IHB Detection | No |
Blood Pressure Risk Indicator | No |
Average Last 3 Results | No |
Included Cuff Size | 22.0-36.0cm ( 8.6''- 14.2'' ) |
Low Battery Detection | YES |
Automatic Power-off | YES |
Power Source | 4 “AA” or AC Adapter |
Battery Life | About 2 months (test 3 times per day, 30 days/per month) |
Backlight | No |
Talking | No |
Bluetooth | No |
Unit Dimensions | 16.2X11.0X6.2cm |
Unit Weight | Approx. 405g |
Packing | 1 pc / Gift box; 24 pcs / Carton |
Carton Size | Approx. 40.5X35.5X42cm |
Carton Weight | Approx. 14kg |
• 24 years of OEM & ODM expertise.
• 3 manufacturing centers with 260,000㎡ automated facilities and 2000㎡ automated warehouses.
• 30+ production lines & 100+ patented innovations.
• ISO 13485, MDSAP, BSCI certified quality systems.
• Full customization for global brands, including Fortune 500 partners.

• WHX Dubai (formerly Arab Health), Dubai
• WHX Miami (formerly FIME), Miami, USA
• Hong Kong Electronics Fair, Hong Kong
• ABC Kids Expo, USA
• KIMES, Seoul, Korea
• MEDITEX Bangladesh, Dhaka
• Hospitalar, São Paulo, Brazil
• Canton Fair, China
• MEDICA, Düsseldorf, Germany
We are committed to meeting partners worldwide at leading international medical and consumer health exhibitions.

Q1: What are the specific benefits of having both FDA and MDR CE certifications for our sales in different markets?
A1: This is a key advantage for expanding into global markets. FDA certification is an authoritative endorsement for entering the North American market (USA, Canada, etc.); while MDR CE certification is proof that the product complies with the EU's latest and strictest medical device regulations, a legal prerequisite for entering the European market. Holding both certifications means you can purchase the same product and compliantly sell it in these two largest global medical device markets simultaneously, greatly simplifying your supply chain and compliance management.
Q2: How should the 4x30 memory design be allocated reasonably in practical use?
A2: This design offers high flexibility. The most common allocation is reserving one memory group for each of four core family members (e.g., parents, grandparents), keeping data completely separate. In clinical or pharmacy settings, it can also be set as three fixed user groups plus one public test group, balancing long-term patient tracking with temporary testing needs for clear and efficient management.
Q3: As a purchaser, does this multi-certified product imply higher cost and pricing?
A3: Obtaining authoritative certifications indeed means higher investment in product R&D, testing, and production to ensure quality. However, from a commercial perspective, it saves you potential market access risks and time costs. You can leverage these certifications as a core selling point, targeting channels with higher demands for compliance and professionalism. This supports a more competitive product positioning and premium pricing space, achieving a higher return on investment.
For customized solutions or partnership inquiries, please contact us at marketing@sejoygroup.com to discuss your specific needs.