Rivarp is accredited by the BSI in (ISO 13485 :2016 & 9001:2015), and passed inspection of Good Manufacturing Practice for Medical Devices. Rivarp Medical’s Manufacturing facility is approved for Class-A, B, C and class D medical devices by the licensing authority Central Drug Standard Control Organization (CDSCO).
In our endeavour to bring the best quality of medical devices and services to humanity, each and every implantable product in our manufacturing unit undergoes six different quality tests before reaching the operating physician.
Spine
Spinal Stabilization system with proven quality standards
Premium Pedicle Screw System
Value Segment Pedicle screw system
Transforaminal Posterior Lumbar Interbody Cage System
Posterior Lumbar Interbody Cage System
Anterior Cervical Plate
Anterior Cervical Cage
Posterior Cervical Fixation
Posterior Cervical Fixation
Posterior Cervical Fixation
Posterior Cervical Fixation
Mechanical Test Results
Biocompatibility Test Results
Cardiology
STRUCTURAL HEART OCCLUSION SYSTEM / STRUCTURAL HEART DISEASES PRODUCT
Heart Occlusion & Delivery System
Septal Occluder
Septal Occluder
Occluder
Delivery System
Cardiology Accessories
Frequently Asked Questions
Every product in the Rivarp stable is made with thorough R & D and developed at our production center based in Bangalore.
We are working on a couple of new products for the Spine and one for Cardiology. We will share updates on these products if any, on our social media handles when they are ready.
Going forward, Rivarp Medical is committed to enriching its product portfolio, improving product quality and enhancing medical services, to provide safe and innovative medical devices for doctors and patients globally and consistently contribute to the development of the industry.
