Quality Management

In our opinion, “A sustainable quality mentality” is the most critical fact for the permanency of a company. The main approach of RD MEDICAL is to maintain high quality products for the long run, an approach which aims at earning trust and building loyalty with our customers who we aim to serve for the long term.

Instead of using these certificates just as keys for trade, we prefer managing our business according the requirements of these systems. ISO 13485:2016 Quality Management System is efficiently adapted on the organization of RD Medical and provides a 100% traceability from initial to final product.

Our main task with respect to Quality Management  is ensuring a complete control in a reliable and continuous production quality with machining, polishing, washing, color anodizing and laser marking units within our organization.

​Biomechanical and biocompatibility tests were performed in accordance with ASTM and ISO standards which are required to launch our products to the market reliably, in addition all Prodorth products are firstly used by our surgeons and only launched to market after  the succesful clinical outcomes are obtained.

RD Medical has identified the problems during surgical operations and contacted surgeons on this issue. These feedbacks and internal discussions, analysis and wide researches provide new approaches which leads to new ideas.

Research and development to offer the innovative solutions will be always the priority of RD Medical to which “R&D” initials were adopted.





Customer Feedbacks

Compliance, Regulations


Research & Development

Transfer of design to production




Conformity of suppliers

Conformity of raw materials

Storage & Logistic

Packaging control

Final quality control


Machining, Cleaning, Anodizing,

Lazer marking control

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All our manufacturing processes are followed up and managed in accordance with the  medical device directive 93/42/EEC and a well-established  ISO 13485:2016 system. At the same time, the transition to the 2017/745/EC Medical Device Regulation (MDR) is in progress.

ISO 13485:2016 IMPLANTS

High Quality

Our job is directly related with human. We unconditionally offer best for human.


Innovation makes the life better, we use different approaches for better solutions.


R&D is always inseparable part of RD MEDICAL , in our commercial name, either in our organization.