Key Information
Main Markets
North America, South America, Western Europe, Eastern Europe, Eastern Asia, Southeast Asia, Middle East, Africa, Oceania, Worldwide
Business Type
Manufacturer
Brands
JHK
No. of Employees
50~150
Annual Sales
10000000-50000000
Year Established
2016
Export Percentage
70% - 80%
Introduction
Services
History
Team
Shenzhen Better Love Medical Technology Co., Ltd. is a professional supplier specializing in original and compatible medical cable connectors, as well as medical electronic equipment accessories and consumables.
- Our comprehensive product portfolio includes disposable and reusable pulse oximeter sensors, ECG monitoring leads, 12-lead EKG machine cables, SpO2 adapter cables, ECG electrode pads, NIBP cuffs, metal connectors, air hoses, medical-grade batteries, equipment modules, humidifier chambers, sampling tubes, ECG/monitor adapter cables, disposable temperature sensors, invasive blood pressure sensor cables, blood pressure cuff kits and various other connecting accessories.
- Our products apply to a wide spectrum of medical instruments, including multi-parameter patient monitors, pulse oximeters, electrocardiograph (ECG) machines, ECG systems, electroencephalograph (EEG) devices, ultrasound systems, fetal monitors and defibrillators. With complete product specifications available, we ensure reliable compatibility with most imported and domestic device models.
- Our products have been exported to more than 60 countries and regions across the globe, and are well recognized and trusted by customers worldwide.
Shenzhen Beijiaai Medical provides comprehensive one-stop solutions for global medical distributors, hospitals and brand partners, focused on high-quality patient monitoring consumables and accessories.
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Full-Range Product SupplyWe offer a complete portfolio of disposable and reusable SpO2 sensors, ECG/EKG cables, temperature probes, IBP cables, NIBP cuffs, defibrillation electrodes, fetal probes and respiratory consumables, with reliable compatibility with mainstream brands including PH-ILIPS, Mindray, Nihon Kohden, Si-emens, Edan, Ma-siMo and Nell-cor.
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OEM/ODM CustomizationBacked by 12+ years of industry experience and two self-operated production facilities, we deliver end-to-end OEM/ODM services covering brand labeling, specification tuning and exclusive product development. All custom projects are governed by ISO 13485 quality systems with flexible MOQ terms.
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Technical & After-Sales SupportOur professional engineering team provides accurate model matching, parameter consultation and full after-sales technical guidance, helping customers resolve compatibility issues and product application problems efficiently.
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Global Delivery ServiceWe support both small-batch trial orders and large bulk purchases. With stable monthly production capacity and mature partnerships with top international logistics carriers, we ensure reliable on-time delivery to over 60 countries and regions worldwide.
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Regulatory Compliance SupportOur core products are certified under ISO 13485, CE (MDR), FDA 510(k) and other global regulatory standards. We provide full certification dossiers and Certificates of Free Sale (CFS) to assist with customs clearance and local market access.
Our Development Journey
Inheriting craftsmanship and advancing through innovation, we have built 12 years of professional expertise in the R&D and manufacturing of patient monitoring medical consumables, with a clear path of steady growth and global expansion.
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2012: Foundation & European Market EntryFounded in Shenzhen with a core focus on compatible SpO2 sensors and ECG cables, we rolled out our first generation of self-developed monitoring consumables. We obtained EU CE certification in the same year, officially entering the European market with products widely recognized for accurate measurement and stable quality.
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2015: Global Expansion & FDA ClearanceWe established a dedicated international business division to develop Southeast Asian, Middle Eastern and Latin American markets, and set up our first overseas technical support station. Our core product line obtained US FDA 510(k) clearance in the same year, successfully opening access to the North American market.
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2018: Full Product Line LayoutWe completed the strategic expansion of respiratory and anesthesia consumables, achieving full coverage of supporting consumables for patient monitoring scenarios. All products are manufactured under strict medical-grade quality standards to meet diversified clinical and commercial demands.
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2021: Intelligent Manufacturing UpgradeWe deployed Industry 4.0 intelligent production lines to realize digital management across the entire production process, with annual output reaching tens of millions of units. We were also certified as a National High-Tech Enterprise in recognition of our independent R&D capabilities.
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2024: MDR Regulatory UpgradeProactively adapting to evolving global medical device regulations, we completed full EU MDR certification for our core product range. This milestone confirms our quality management system meets the latest EU requirements for product safety, full traceability and risk management.
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2025: New Self-Owned Production BaseOur brand-new self-owned production base was fully commissioned, tripling the workshop area and boosting annual production capacity by over 50%. The upgraded facility enables end-to-end quality control, intelligent manufacturing and more stable long-term supply for all global partners.
Guided by the philosophy of "quality first, innovation-driven", we have evolved from a single-product manufacturer to a comprehensive medical consumables solution provider. Today we serve clients in more than 60 countries and regions, and remain committed to delivering reliable, compliant products and professional, efficient services.
Our core team has 12 years of hands-on experience in patient monitoring medical consumables, covering R&D, quality control, international sales and compliance support, to deliver full-range services for medical partners worldwide.
Our R&D team is familiar with compatibility tuning and custom development for all types of monitoring consumables, and can efficiently support OEM/ODM requirements. Our QC team follows ISO 13485 standards across the entire production process, with strict inspections from raw material arrival to finished product delivery, to ensure stable product quality and regulatory compliance.
Our international sales team knows well the rules of regional markets, and provides product selection advice, order follow-up and cross-border logistics support for customers in over 60 countries and regions with smooth, efficient communication. Our compliance staff keep up with regulatory updates such as EU MDR and US FDA, and can provide full certification documents to assist customers with customs clearance and local market access.
All core technical and service staff have received systematic professional training and hold relevant qualifications. We offer multilingual support with prompt response and smooth cooperation.
