LIFELONG MEDITECH PRIVATE LIMITED

Lifelong Meditech Private Limited specializes in single-use medical devices, specifically general-purpose syringes and syringe/needle combinations. These products are designed for common medical procedures like injections, infusions, and sample collection, catering to both clinical and home healthcare environments. The company focuses on simplicity and precision in dosing to meet diverse medical needs.

Lifelong Meditech Private Limited is based in the United States. Since its devices fall under FDA jurisdiction, they are subject to U.S. regulatory requirements, including classification and traceability. The company’s location ensures compliance with local regulations, such as the FDA’s Unique Device Identification (UDI) system, which helps track and monitor these products throughout their lifecycle.

Lifelong Meditech Private Limited’s devices are listed in the FDA’s Unique Device Identification (UDI) database. This registry ensures that each product is traceable and identifiable, supporting compliance with U.S. medical device regulations. The UDI system helps healthcare providers, regulators, and manufacturers track devices from manufacturing to patient use.

Lifelong Meditech Private Limited’s devices are classified as Class II under FDA regulations. This classification applies to products that generally pose moderate risk and require special controls beyond general controls to ensure safety and effectiveness. The classification ensures that these syringes and syringe/needle combinations meet specific regulatory requirements before entering the market.