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Redefining Portable Imaging

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Advancing Medical Device Manufacturing

Our Commitment

Setting New Standards in

Medical Device Manufacturing

Lourdes Lifecare 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.

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Lourdes Lifecare

At Lourdes Lifecare, we design, develop, and manufacture advanced medical devices that are built to enhance, nurture, and preserve life.


Driven by a commitment to quality, innovation, and integrity, we follow world-class standards and ethical practices in every aspect of our operations — from research and engineering to manufacturing and service.

 

We take pride in delivering

“Global Quality with Make in India for India and for the World.”

Our Manufacturing Process

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Design & Engineering

We start with user needs and risk analysis, transforming them into designs that are carefully reviewed, tested, and validated before moving into production.

QMS - Aligned Quality System

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.

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Supplier & Material Controls

Only approved, qualified suppliers provide raw materials and components. Incoming inspections ensure compliance with our strict standards.

Controlled Manufacturing

Each step of production is validated and documented, from assembly to sterilization, ensuring consistency across every device.

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Calibration & Testing

We use validated test methods and calibrated equipment so that every measurement and performance check is accurate.

Traceability & Records

Our Device Master Records (DMR) and Device History Records (DHR) provide full traceability, proving each unit is built to spec.

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Labeling & Packaging

Devices are packaged to protect against damage, labeled with UDI (Unique Device Identifier), and shipped ready for global compliance.

Post-Market Vigilance

We monitor device performance in the field, respond to customer feedback, and implement corrective and preventive actions (CAPA) to continuously improve.

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