Our Commitment
Setting New Standards in
Medical Device Manufacturing
Lourdes Lifecare UK is committed to advancing healthcare through cutting-edge medical devices and integrated services. Our team is dedicated to setting new standards in reliability, performance, and patient safety, empowering healthcare providers with innovative solutions that improve patient outcomes.
Lourdes Lifecare
Lourdes Lifecare UK develops and delivers advanced medical technologies designed to enhance, nurture, and preserve quality of life.
Built on world-class engineering practices, integrity, and exceptional service, we support healthcare innovators in bringing reliable solutions to market.
We go beyond manufacturing—offering end-to-end engineering and commercialisation support, including design, development, prototyping, testing, compliance and regulatory guidance, ERP customisation, project management, certification, and go-to-market strategy.
Our Manufacturing Process
We start with user needs and risk analysis, transforming them into designs that are carefully reviewed, tested, and validated before moving into production.
Design &
Engineering
Only approved, qualified suppliers provide raw materials and components. Incoming inspections ensure compliance with our strict standards.
Supplier &
Material Controls
We use validated test methods and calibrated equipment so that every measurement and performance check is accurate.
Calibration &
Testing
Devices are packaged to protect against damage, labeled with UDI (Unique Device Identifier), and shipped ready for global compliance.
Labeling &
Packaging
Our Quality Management System complies with 21 CFR Part 820 (QSR) and is transitioning to the new FDA Quality Management System Regulation (QMSR), aligned with ISO 13485.
FDA-Aligned
Quality Systems
Each step of production is validated and documented, from assembly to sterilization, ensuring consistency across every device.
Controlled Manufacturing
Our Device Master Records (DMR) and Device History Records (DHR) provide full traceability, proving each unit is built to spec.
Traceability &
Records
We monitor device performance in the field, respond to customer feedback, and implement corrective and preventive actions (CAPA) to continuously improve.
