Lub Dub Medical Technologies was founded in 1994 by visionary Biomedical Engineer Mr. S. Appasamy, after identifying that over 75% of medical device failures were caused not by machines—but by their accessories.
At a time when critical medical accessories like ECG cables, SpO₂ sensors, NIBP cuffs, breathing circuits, and ultrasound probes were almost entirely imported, Lub Dub took the bold step of localizing production in India.
Today, Lub Dub is more than just a medical accessories manufacturer—we are a trusted OEM partner, NABL-accredited calibration lab, and a nationwide distributor of biomedical test equipment and training manikins.
At Lub Dub Medical Technologies, quality and compliance are non-negotiable. We proudly hold:
At Lub Dub Medical Technology, quality and compliance are non-negotiable. All our systems—from design and manufacturing to calibration and servicing—follow stringent quality norms and international standards.
We are proud to be:
NABL Accredited for biomedical equipment calibration
ISO-certified for our processes and quality management
A registered MSME and recognized partner to several hospital chains and medical institutions
Our certifications stand as proof of our commitment to precision, reliability, and safety.
To become India’s most trusted biomedical brand, delivering innovative, high-quality, and affordable healthcare technologies made in India.
We aim to reduce dependency on imported accessories by offering locally manufactured solutions that meet global standards. Our goal is to support hospitals, clinics, and biomedical professionals with products and services that improve patient care, safety, and efficiency.
At Lub Dub, we strive to make cutting-edge medical technology accessible to all, while building a healthier and self-reliant India.
Trusted by hospitals, biomedical engineers, and healthcare professionals across India. Real feedback from those who trust Lub Dub
FAQ
Under the Medical Devices Rules 2017, manufacturers, importers, and distributors must comply with various CDSCO licensing and registration requirements depending on device classification.
MD-13 – Test License for Manufacturing
MD-17 – Test Import License
These licenses are applicable for testing, evaluation, examination, and demonstration purposes.
MD-5 – Manufacturing License for Class A & B Devices
MD-7 – Manufacturing License for Class C & D Devices
The license category depends on the risk classification of the medical device.
MD-15 – Import License
Required for importing notified medical devices into India.
CDSCO Registration Number
Applicable for Class A non-sterile and non-measuring devices.
MD-42 – Sale & Distribution Registration
Required for authorized sale and distribution activities.
FSC – Free Sale Certificate
MSC – Market Standing Certificate
NCC – Non-Conviction Certificate
These documents support regulatory approval and compliance processes.
Choosing the correct CDSCO regulatory pathway helps avoid delays, ensures faster approvals, and maintains compliance with Indian medical device regulations.
Explore our high-quality accessories, simulators, and NABL-certified services.