Approved for Class A to D devices.
Rivarp Medical Pvt. Ltd. has a state-of-the-art production facility in Bengaluru, Karnataka, approved by the Central Drugs Standard Control Organisation (CDSCO) for manufacturing Class A, B, C and D medical devices.
Stringent standards at every step.
The facility adheres to stringent quality control standards, ensuring that each product undergoes multiple quality tests before reaching healthcare professionals. Accreditation to ISO 13485:2016 and ISO 9001:2015 reflects our commitment to high standards of quality and safety.
- CDSCO-approved for Class A, B, C and D medical devices
- ISO 13485:2016 medical device quality management system
- ISO 9001:2015 quality management system
Certified and approved.
Quality and regulatory accreditations held by Rivarp Medical.
BSI
ISO 13485:2016
CDSCO · Class A–D manufacturing
US FDAInnovative devices that meet every requirement.
Rivarp Medical Pvt. Ltd. is committed to providing innovative medical devices and equipment that meet our customers’ requirements and applicable regulatory and statutory requirements. We maintain an effective quality system by managing product and process risk. The quality system is reviewed for continuing suitability by executing objectives related to:
- Product development and improvement
- Quality system planning and improvement
- Supplier quality assurance
- Personnel training and competence
- Applicable regulatory compliance and internal / external audits
- Process effectiveness and efficiency
The backbone of Rivarp.
R&D is a complex, iterative process that drives innovation and the creation of effective, safe, physician-friendly and patient-centric healthcare solutions.
Need our certificates?
Contact us for copies of our ISO and CDSCO documentation for tenders, registrations and distributor qualification.