(ISO 13485:2016)
Manufacturer of Non-Active Surgical, Dental Instruments and hollowware
(ISO 9001:2015)
Manufacturer of Surgical, Dental, Veterinary Instruments and hollowware
(cGMP 21 CFR Part 820)
Manufacturer of Non-Active Surgical, Dental Instruments and hollowware
Sambrialmed International® was established in 2015.
Sambrialmed International® is striving hard to keep pace with the new developments in the surgical field. We manufacture and export different types of Non-Active Surgical,Dental, Veterinary instruments and Hollowware. Fourth generation or you can say a century,
Sambrialmed International® have been occupied with manufacturing of quality medical products especially surgical instruments of which we are catering the products for every specialty.
Sambrialmed International®explored the world market in a very short time with complete customer satisfaction.
Sambrialmed International® is manufacturing and exporting medical devices intended for human use in such a manner that they are safe and in compliance with international standards practices i.e. ISO 9001:2015, ISO 13485:2016, cGMP 21 CFR Part 820 & Medical Device Regulation (MDR) EU 2017/745. Our main objective is to produce medical devices intended for human use in such a manner that they are safe and in compliance with the applicable Standards.
Sambrialmed International® is utilizing modern techniques and profoundly technical skilled workforce of one hundred and sixty (160) people to carry on its expanding manufacturing activities. Company export has been gradually increasing over the year.
Sambrialmed International, abide by all the applicable regulatory national & international laws related to the
welfare of employees as well as occupational health and safety management system.
OUR GOALS
HIGH QUALITY INSTRUMENTS
COMPETITIVE PRICES
TIMELY DELIVERY
CONSISTENCY OF PRODUCTSSambrialmed International® has made the “Strategic Business Decision” to develop and implement an effective Quality
Management Systems (QMS) for Medical Devices across all functions of the Company. Organization involved in one or more stages of the life cycle of a medical device i.e. production, storage and distribution. Suppliers or other external parties providing product (e.g. raw materials, components, subassemblies, semi-finished medical devices and process services, calibration services, distribution services, maintenance services) to organizations can also use the guidelines and principles in this QMS Manual.